Podcast: Policing Language in Mental Health Communities



In the first full episode of Not Crazy, we learn a little more about the new co-host, Jackie, and her history with chronic illness and depression. Gabe rants about person-first language and how nitpicking verbiage is distracting from more pressing matters in the lives of those living with mental illness.  Overall, we decide that “crazy” is not a dirty word and there are other, more time-sensitive, things we should be focusing on that can benefit the mental health community. 

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About The Hosts

Gabe Howard is an award-winning writer and speaker who lives with bipolar disorder. He is the author of the popular book, Mental Illness is an Asshole and other Observations, available from Amazon; signed copies are also available directly from Gabe Howard. To learn more, please visit his website, gabehoward.com.

 

Jackie Zimmerman has been in the patient advocacy game for over a decade and has established herself as an authority on chronic illness, patient-centric healthcare, and patient community building.

You can find her online at JackieZimmerman.coTwitter, Facebook, and LinkedIn.

Computer Generated Transcript for ‘Policing Mental Health Language’ Episode

Editor’s NotePlease be mindful that this transcript has been computer-generated and therefore may contain inaccuracies and grammar errors. Thank you.

NC – Ep 1 Policing Language

Gabe: [00:00:00] Welcome and you’re listening to Not Crazy with Jackie Zimmerman. She is depressed and colostomy-ized.

Jackie: [00:00:07] I don’t know if I should introduce you yet because you already got it all wrong.

Gabe: [00:00:10] I mean, you’re not depressed at the moment, but.

Jackie: [00:00:12] No, but I also am not colostomy-ized. That’s wrong. This is Gabe Howard, he’s bipolar. He also has no idea what a colostomy is. And that I don’t have one.

Gabe: [00:00:22] But you have a J bag

Jackie: [00:00:24] I have a J pouch.

Gabe: [00:00:26] What’s the difference, isn’t a pouch and a bag like the same thing?

Jackie: [00:00:29] No. A J pouch is an internalized thing made out of your small intestine, an ostomy bag is an external device made out of not your intestine.

Gabe: [00:00:41] I really think there’s a missed opportunity here. They should reverse that. They should make the external one out of your intestine. Because think of the discussion that you could have like, oh my God, what’s that? Oh, it’s my small intestines strapped to the side.

Jackie: [00:00:55] Well, actually, if you want to if you want to get technical. Although I feel like it’s a bit off-topic, however, a stoma is made out of your small intestine and does sit on the outside of your abdomen. So when you do have an ostomy, you do get to see part of your intestine on the outside of your body.

Gabe: [00:01:11] You’re fun at parties.

Jackie: [00:01:13] So weird party trick. Yeah. Yeah.

Gabe: [00:01:15] I’m really excited. Our first episode ever. We’re just getting to know each other. This is the first recording, so it’s not like we did a whole bunch of practice and then recorded our first one, which now that I think about, it would have been like a really good idea.

Jackie: [00:01:27] Probably,

Gabe: [00:01:28] Yeah

Jackie: [00:01:28] Yeah

Gabe: [00:01:28] We could have started off a lot stronger. I feel like we need a Jackie joke in there.

Jackie: [00:01:33] I don’t have one.

Gabe: [00:01:34] Make up a joke.

Jackie: [00:01:36] I can’t be joking on the spot. I’m not funny on the spot.

Gabe: [00:01:39] So you’re only funny accidentally.

Jackie: [00:01:42] Yes. Yes. Yes. When I first met my husband, I told him that I’m the funniest person he will meet. And he said, Oh, tell me a joke. And I said, I don’t tell jokes. And I was like, I don’t understand. Like, I’m just really funny, but I don’t tell jokes. So it’s like no pressure.

Gabe: [00:01:55] My ex-wife thinks that she’s funny because people are constantly laughing at her. But yeah, it’s never on purpose.

Jackie: [00:02:03] Oh.

Gabe: [00:02:03] She is being very serious and I should point out that I am good friends with my ex-wife. I mean, she was still smart enough to divorce me. This is a mental health podcast, and the reason that we picked the great Jackie Zimmerman to be the co-host of Not Crazy is because you just have such an incredible wealth of physical health knowledge. And I have such a wealth of mental health knowledge. And what we found out sort of during our preproduction and getting to know each other and interview stage is that you ignored your mental health because you were so focused on your physical health. And I ignored my physical health because I was so focused on my mental health.

Jackie: [00:02:43] Together, we could have been one whole person.

Gabe: [00:02:45] One whole person. Would we have been like short with blue hair or tall with red hair, like what would our person have been?

Jackie: [00:02:53] We would’ve been a medium with purple hair.

Gabe: [00:02:56] I want that so badly.

Jackie: [00:02:59] That’s some color theory right there.

Gabe: [00:03:01] As you know, this is the offshoot of A Bipolar, a Schizophrenic, and a Podcast. That was the start of this whole idea that the idea that people with mental health issues, people living with mental illness, whether it be schizophrenia, bipolar depression or just, you know, grief or anxiety or OCD or just, shit, I had a bad day and I don’t know how to deal with it needed an outlet. They needed to hear about stuff that was important to them and not like in this nonsense self-help garbage. Oh, you’re a shitty person, but if you listen to my podcast and give me a hundred dollars, you’ll be less of a shitty person kind of way.

Jackie: [00:03:34] But if you do want to give us one hundred dollars, I wouldn’t be sad about it.

Gabe: [00:03:37] We will not turn down one hundred dollars. You can PayPal us at show@psychcentral.com. That’s not even a real PayPal address, like the money is going to go nowhere. So, so, so quick. What what’s our what’s our PayPal address, Jackie? No, just kidding. Don’t say it. Don’t say it

Jackie: [00:03:53] I think part of the will say inspiration behind this show and the direction that we’re taking is this idea that physical health and mental health are connected, but that the world doesn’t quite realize that. So there’s a lot of focus on physical health about how to keep yourself fit and great and all of this stuff. And they’re starting to become, I would say, a shift on mental health. But there still is a lack of understanding that mind-body connection. It is real. And as somebody like myself, like we mentioned, had a very rough go at physical health, not just like I wasn’t healthy and I was overweight and sad and lonely. Well, that’s not physical. But, you know, I mean, it was that like my body was eating itself and I was dying. It’s kind of this bizarre thing that you’re talking to a doctor. You still have to really push the mind-body connection. I have a medical team now that believes this, which was a huge shift from when I first was sick. And so I think the idea behind this podcast is to talk about mental health from people who obviously are mentally ill. I guess we’ll talk about that later, because I don’t really define as mentally ill, however, but not discounting the fact that a lot of people with physical disabilities, physical illness, also experience issues with their mental health and not discounting their experiences by saying, oh, well, it was just a temporary lapse of happiness in your life or it was just situational depression, like all of those are issues with mental health that are worthy of being addressed.

Gabe: [00:05:27] I love what you said, even though you have depression, even though you’ve been suicidal, even though you take medication for depression, you don’t define as mentally ill. So, for example, even though I am 42 years old, I don’t define it as 42 years old. I define as a millennial because everybody hates me. So it just seems like it fits better. And you’re probably thinking as a millennial, no gay, but you are not a millennial, just like I’m thinking. No, Jackie, you’re not mentally healthy.

Jackie: [00:05:59] Yeah, I think that’s a pretty fair assumption because I am 100 percent thinking that.

Gabe: [00:06:03] The way that we talk about mental health, mental illness, the word that we use, we see a lot of stuff on the Internet about everybody policing language. And it’s not just in mental illness. It’s not just in mental health. It’s it’s everywhere. Everybody is just fighting about, you know, person-first language. These words are offensive. I don’t identify that way. Don’t talk it this way. I’m not trying to throw that all out. Like these aren’t valid discussions because I think that there are valid discussions in there. But I think that sometimes people go too far. And speaking just in the mental health community, we have this idea that people who say things like I am bipolar are somehow being offensive

Jackie: [00:06:49] Yes.

Gabe: [00:06:49] Or people who say I’m not crazy or I am crazy or I feel crazy or I’m acting crazy like, no, no, no, we can’t say crazy.

Jackie: [00:06:57] Or even just using the word crazy like, oh, that’s crazy. You can’t say crazy. I am guilty of this. I say bananas. I don’t say crazy. Makes it feel icky. So I’ll be like, oh, that’s bananas. And it’s also because I picked up from a former co-worker who I really liked.

Gabe: [00:07:12] But here’s the problem that I have with this. We’re not doing shit to make life better for crazy people. We’re just changing what we call them. Isn’t that fantastic? We don’t have to do anything to make you well. But we’re going to give you a different name.

Jackie: [00:07:27] When we started being more p.c. and making things better for them because you can’t call them crazy. We gave them a better title, we’ll say. But then we took away all their help and support. So their lives got shittier

Gabe: [00:07:38] Do you think that people in those families feel like that’s a win? Do they really feel better that they can’t get the medical care that they or their family members need? Because after all, we’re speaking about them in a positive way. We’re not putting our money behind them in any positive way, but we’re speaking about them in a positive way.

Jackie: [00:07:58] So. No, I live in Michigan and I saw in the news the other day. We are rolling back resources for mental health. Michigan State wants to shut down funding for counselors to meet with patients via insurance. So basically in a time where Generation Z, we’re all crazy, all the little ones are running around with their lives on display and freaking out about it. That wasn’t very nice. But anyway,

Gabe: [00:08:24] You’re getting letters for that one.

Jackie: [00:08:26] I know. I’m sorry. I’m not sorry anyway.

Gabe: [00:08:28] I apologize. Wait, wait, hang on. It’s Generation Z?

Jackie: [00:08:32] Yeah.

Gabe: [00:08:32] You’re getting tweets for that one.

Jackie: [00:08:33] Yeah,

Gabe: [00:08:33] You’re getting insta pictures for that one.

Jackie: [00:08:36] They’re going to Snapchat me, but joke’s on them, I’m not Snapchat. But there’s this there’s this huge focus. I mean, all the psychologists and psychiatrist are saying we are about to have a mental health epidemic on our hands with this next generation. And meanwhile, our legislatures like cut the funding. We’re fine.

Gabe: [00:08:52] We’ll be right back after this message from our sponsor.

Jackie: [00:08:55] And we’re back talking about why crazy is not an offensive word.

Gabe: [00:08:59] I’m always going to say things, quote unquote, correct. You know, I’m going to say died by suicide rather than committed suicide. I understand how person first language works living with bipolar or living with schizophrenia. I understand all of these things because. Well, I’ve been educated. I’m right in the thick of things. You might not know this, but I have a podcast.

Jackie: [00:09:19] You have a couple podcasts.

Gabe: [00:09:21] I do, I do, and they’re fantastic, but I didn’t start out this way. And could you imagine if Gabe Howard from 20 years ago would have gotten the courage fuck. Could you imagine if Gabe Howard from 20 years ago would have gotten the balls to stand up and say, hey, something is wrong with me. I am crazy. I am screwed up. And the response to that would have been, “Gabe, but no. You’re a person who is living and currently experiencing a mental health issue. You’re saying it all wrong.” You know how much gumption and courage it takes to admit that you’re crazy. And instead of helping me with that, they corrected my language.

Jackie: [00:10:05] I can’t relate to that necessarily because my issues with depression and anxiety didn’t start until my mid 20s when I was an adult and supposed to be living my life and being great. And then I got sick in my life just like tanked really fast. I lost my job. I was dying all that jazz, you know, that fun stuff. But I didn’t even really have the opportunity to sort of declare that I was depressed. I just got there real fast and it got real bad, real fast. And there was no talking to people to get help. It was just this is a crisis immediately. We need to jump on this before there’s nothing left to jump on. So I remember one time I was really, really sick and I was really, really depressed. And I was definitely planning my suicide. And I went to my doctor for a regular checkup and my dad drove me because I wasn’t able to drive myself. And the doctor was like, we need to get you inpatient like right now. I was like, but I have this day planned with my dad. And he drove me here. And I really just want to spend the day with my dad. And she basically was like, well, if you’re going to stay with your dad, that’s fine. And in hindsight, I’m like, was that the right decision? I’m still here. So I guess it worked out fine. But the idea of I guess that was me asking for help or asking for definition or asking for someone to give me something. And she was like, here with your dad, it’s cool. Mind you, I was twenty five. It’s not like I was 16. But it was weird to me that she was willing to let somebody who just said, I am suicidal and very, very, very depressed because my life is getting worse with my sickness. Just go home. She was all right bye

Gabe: [00:11:43] There’s so much to discuss in that statement. You actually use the correct words. You said, I’m suicidal, I’m depressed and still you got sent home. So imagine what would have happened if you would have walked in and said, I’m crazy and I’m going to kill myself,

Jackie: [00:12:01] Yeah.

Gabe: [00:12:01] Especially as a woman. You know, listen, women and millennials at that are always labeled dramatic. So if you would have said, I hate my life, I want to kill myself, but I want to die. And they would’ve been like, oh, god, another woman with blue hair and tattoos screaming that she wants to die. It’s unfortunate, but the care that people with mental illness get is just so incredibly dependent on stereotypes. It’s so incredibly dependent on the amount of money that we have. They always say that the difference between crazy and eccentric is a million dollars.

Jackie: [00:12:36] Whoo! Good one.

Gabe: [00:12:38] But why? You realize that some of these famous artists throughout history that we look at, Andy Warhol is my favorite. This guy was fucking nuts. He literally boxed up his tissues and toilet paper and required them to be warehoused. But he was eccentric. He was unique.

Jackie: [00:13:00] Well, and I would also argue in the same same category of millionaire. He gave the world art so they can say, look at his beautiful art. Artists are eccentric versus me or you. I mean, technically, I have an art degree, but I don’t really do art. So his value was high because he was an artist. So his crazy didn’t matter because he was valuable.

Gabe: [00:13:21] And when does that shift? When does that shift over? Like, for example, if you start making art tomorrow. Jackie, I’m going to assume that you’re not going to become Andy Warhol. No offense. Just no offense.

Jackie: [00:13:33] None taken.

Gabe: [00:13:34] But you are creating art. So does this mean that we’re going to allow you to wipe your ass, put it in a box and store it in your garage and we’ll just call you eccentric? Or are the people listening to this thinking, that’s bat shit crazy. Saving that is disgusting and sick and that person needs help. But Andy Warhol not only did that. He paid people to do it for him. He just

Jackie: [00:13:58] Well, that’s where the money comes in.

Gabe: [00:13:59] He just putut the box. And now, all these years later, we open up these boxes and sort through them. And we’re finding fascinating things in there,

Jackie: [00:14:09] Like shit.

Gabe: [00:14:09] Like Polaroids of Marilyn Monroe, and shit.

Jackie: [00:14:13] Well, this is this is the perfect storm trifecta of the appropriate type of crazy. The I contributed to the world. I have a lot of money and I’m crazy. And if you are missing any of those pieces, I don’t think it works. I don’t think you get to be Andy Warhol. If you’re not rich or you’re not an artist.

Gabe: [00:14:33] So it means that we’re not policing the behavior anymore. And that’s my entire point. We’re not looking at the behavior. We’re looking at the person and then the behavior. This behavior is OK if you’re Andy Warhol. This behavior is not OK. If you’re Gabe Howard, but this behavior becomes OK again. If you’re homeless suffering from schizophrenia and we’re OK with letting you freeze to death under a bridge because after all, get a job, lazy ass.

Jackie: [00:15:00] Well, because now you’re doing the opposite. You’re not contributing. You’re doing the opposite, you’re hurting us. So we don’t need to help you.

Gabe: [00:15:06] Shame on you and your homelessness.

Jackie: [00:15:08] Right. This is your fault.

Gabe: [00:15:10] The discussion surrounding severe and persistent mental illness is almost non-existent until a crisis point happens. The discussion surrounding mental health and mental health crises are starting to to happen in a productive way. But we have all of these external forces that are trying to control the narrative by controlling the words. The example that I get all the time, as I say, my name is Gabe. I’m bipolar. And people immediately look at me and say, no, you’re not. You’re so much more than just bipolar, Gabe. You’re a person to which I respond. Yeah, I know that. Do you think so little of me that you think that? I think that I’m just bipolar. Also, why are you hearing the word just. I said I’m Gabe. I’m bipolar. And what you heard was, I’m Gabe. I’m just bipolar. Why did you feel like you needed to add that word? If I would have said I’m Gabe, I’m married. Would you have said, oh, my God, you’re so much more than just a husband? If I would have said, my name is Gabe, I’m a father. Oh, my God, you’re so much more than just a father. Come on. If you introduce yourself. Hi, I’m Jackie. I work with Gabe. Do you think anybody would say, oh, my God, Jackie, you do so much more than just work with Gabe. You are much more than that. And if they did say that, would you reply? Oh, my God. I didn’t realize that I had more worth than just my partnership. The bipolar dude I met on the internet. How effective is that? Isn’t that mansplaining? It’s like mental illness plaining.

Jackie: [00:16:37] It is, and it actually goes across condition areas, whether it’s mental illness, physical disability, chronic illness, this kind of thing is rampant everywhere. I’ve been doing a lot of research in the physical disability space research meaning, I follow a lot of people on Twitter who are talking about this and how people are working really hard to remove the term sort of. I am disabled from their vocabulary and the people these advocates in the disability space are saying why you are disabled like that. That is part of who you are. And by removing it. It’s adding the stigma that it’s bad to be disabled. So by saying I’m disabled, that means we all think it’s bad. So you identify that way. So we think you’re bad. So we don’t like you because you’re disabled. And I think that this goes across the board and mental illness or chronic illness. For example, I have multiple sclerosis. I don’t identify as disabled because of that, which is another weird. You know, what I identify as is becoming apparently clear that I don’t identify in any of the right ways, but I have multiple sclerosis. I’ve always said that the phrase I have multiple sclerosis, it doesn’t have me drives me fucking insane. I hate that shit because the thing is, I do have it. I will always have it. It’s not going to go away. Is it all that I am? No. Like you said, it’s not. I think the move to do this. The idea was to do the I am not just this. That was the idea behind person first phrasing was I’m not just to this one thing, but by changing it, we are actually removing the power by identifying this way. And I’m not gonna say I feel powerful when I say I have M.S. or I have ulcerative colitis or I have depression or I have anxiety, should I keep going? And all the things that I have, I’m not going to say.

Gabe: [00:18:22] We don’t have that kind of time.

Jackie: [00:18:23] I don’t feel more powerful when I say that it’s not a conscious decision, but it just seems silly to me to beat around the bush to say I’m a person with or I have been diagnosed with. No, I have it. End of story. It’s faster. It’s I guess it’s it’s a more compact way of saying it. And I’m all about getting shit done fast.

Gabe: [00:18:40] For me, it’s just about wanting to define my own life. That’s all I’ve ever wanted to do. I remember Gabe at Wales. I was a fat, little pimply faced, four eyed, braces having, redhead.

Jackie: [00:18:56] Face only a mother could love.

Gabe: [00:18:58] Oh, my God. I don’t even think my mother loved it, to be honest. She was just like, oh, my God. He’s adopted. I was. My parents just I don’t know. And I’ve long since lost the point of this entire story.

Jackie: [00:19:13] Let me reel it in for you. I got this. Ready. So the experiences of young Gabe led you to this point. You did not have a diagnosis to to, I guess, attribute some of your behaviors to. Now you do. And the lack of, let’s say, attention to that or treatment of that, develop some behaviors in you that took you into adulthood and took you into this space where you want to advocate for bipolar, which also puts you in a space to be a well-known advocate for bipolar, which I think means to some extent does make bipolar a huge part of who you are. And part of your identity. I feel the same way. Like as an advocate for M.S. and you see and I have been in this space for 14 years. When people say I have a message doesn’t have me or, you know, I’m more than just M.S., nope. This is a huge part of me. I make my career. I’m talking about having these things like if I didn’t have these things, I wouldn’t be here. I would be talking about it. It’s not the only part of my identity, but it is a huge part of who I am. I make money on it. It’s a massive part of who I am.

Gabe: [00:20:21] I thought you you’re gonna say you make massive money and I was about to hit you up for a loan.

Jackie: [00:20:24] No. No.

Gabe: [00:20:25] So, I’m sorry that.

Jackie: [00:20:26] I don’t. Let me correct that. I do not make massive money on this. I just make some money on this.

Gabe: [00:20:32] I’m not trying to get the whole world to use the correct language so that people can get help. I’d much rather focus on what people are actually saying. I read this fascinating article that said that if your child says they have a stomach ache all the time and by child, you know, like, you know, four, six, eight. But if your child is constantly saying, I have a stomach ache, they might not actually have stomach problems, they might have anxiety. But kids don’t have the words for anxiety. They don’t have the words for nerves. They don’t have the words for panic or paranoia. What they do have are the words to describe stomach ache. I feel that it would be much better to educate the parents and the adults that I have a stomach ache could mean these other things. That person first language really strikes me as no, no, no, no, no. We have to teach a 4 year old to say, Mama, Poppa, I’m having a serious anxiety problem or possibly panic or paranoia, and I must see my mental health specialist as quickly as possible. I think that people lie awake at night and think they’re going crazy. I think people lie awake at night and cry and wish they were dead. I don’t think that people lie awake at night and wonder about the state of their mental health. I don’t think that’s the way that our brains work. I don’t think those are the words in our internal monologue. I don’t think that’s the way that we talk to our friends and our family when we’re desperate and in those vulnerable, vulnerable moments. And if we wipe out all that talk, what’s left? These people are not going to be able to get help because we will not recognize their words or worse, we’ll spend our time correcting them rather than helping them. It stifles.

Jackie: [00:22:10] And on top of the issue with children. So, yes, children do not have these words. But let’s be real people who are not highly educated, affluent and have money for therapy and doctors may also not have these words.

Gabe: [00:22:22] Oh, yeah.

Jackie: [00:22:22] So we’re not just isolating small ones with tiny vocabularies. We’re isolating a large portion of the country we live in who does not have access to care, does not have a great education, does not have higher education. All of these things that give us the verbiage to say what you just said, it’s part of why we nameed the show “Not Crazy.” It’s part of why we did and probably will get more pushback on using the term crazy when talking about people with mental illness. It all comes down to words have weight. If we give them weight. So if you’re offended by crazy, use a different word. If you’re not offended by crazy. More power to you. Here’s the thing. I am a 34 year old suburban, white, straight hetero woman. I’ve got privilege coming out of my ears, which in today’s day and age means I am offended by everything. I’m offended for you. I’m offended by you. All these people I don’t even know. I take offense for them because it’s like my duty in the world we live in right now. I am not offended by the word crazy. And I think part of that is because that’s the word a lot of people know. It’s how they can explain what they’re feeling, what they’re thinking. And if people who don’t identify with mental illness use the term crazy in a way that does not talk about mental illness, it’s not even related to mental illness. Who cares? Right now, I feel like we have bigger issues in the world than whether or not the word crazy is offensive.

Gabe: [00:23:50] And one of those issues is that people with severe and persistent mental illness are literally freezing to death every winter. I don’t really think they care what you call them as long as they can get access to shelter, food and medical care. I’d really love to see us put our resources there rather than policing language.

Jackie: [00:24:10] Snaps. I agree.

Gabe: [00:24:12] But hey, I can’t wait for the day that we have so much money that everybody with a mental health issue gets the help that they need. Everybody fully understands and there’s literally nothing left but to argue about language. And that’s what the Internet was made for. We’re just ahead of our time. Jackie, this was fun. Did you have a good time hosting your first episode of Not Crazy?

Jackie: [00:24:36] I did. I look forward to talking about crazies, myself included. Maybe by the end of this whole thing I will identify as mentally ill. I don’t know, TBD.

Gabe: [00:24:46] We’ll see what we can do for you. All right, listen, everybody, this is our first episode of the Not Crazy podcast. We would love it if you would share us on social media. Post a message if you have any questions you’d like to ask us. You can hit up the same email address. The new Web site for the show is PsychCentral.com/NotCrazy. You can find us on every single podcast player. And as we say goodbye to A Bipolar, a Schizophrenic, and a Podcast, you now have a bipolar, a millennial and a podcast. Frankly, I think we were doing better with the schizophrenic. We’ll see everybody next week.

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8 Ways to Navigate Change Without Stress & Anxiety

Change doesn’t have to be terrifying!

Life change — and change in general — is certain to happen. According to the Greek philosopher, Heracleitus, “The only thing that is constant is change.”

If this is true, and I believe it is, coping with life changes, transitions, and the stress and anxiety that comes with it should come more easily to everyone, don’t you think?

Yet, many shudder at the thought of change. Some bury their heads and hope it will go away while others open their arms and welcome the opportunities.

Heracleitus’ philosophy is a good starting point for those who shudder and duck and cover when they face a major change in life. It may help to do a little reframing and think about change differently.

One way to approach change is to go with the flow. Enjoy the ride, as wild as it may be.

This, of course, is easier said than done when you’re coping with life changes and transitions.

Here are 8 easy ways you can embrace change in your life and make it work in your favor:

1. Accept That Change Is Unavoidable and Uncontrollable.

There are so many different kinds of change in life. Some are expected and can be planned for, such as graduations, having a baby, empty-nesting, or retirement. Most of these are happy circumstances and you wouldn’t want to miss them.

And some come without warning — sudden illness, accidents, or the loss of someone important in your life. These you could do without.

Most people experience many of these life-altering moments in their years on Earth. The ones you can plan for are easier to accept, while those that come out of the blue can knock you upside down and require a lot of recovery time.

Coping with life changes and transitions like these are made easier when you accept that much of what happens is not within your control. Take control of what you can, and let the rest go. The Serenity Prayer is one of my “go to’s” when I’m feeling out of control.

God, grant me the Serenity to accept the things I cannot change, have the courage to change the things I can, and the wisdom to know the difference.

How to Take Control of Your Mind & Eliminate Stress So You Can Live Your Best Life

2. Figure Out How to Manage Your Stress.

Regardless of how the changes in your life happen, the mere experience of the event can change you profoundly. Think about how divorce, whether you asked for it or not, can cause you to wonder who you are now that you’re not Mrs. Somebody.

Your friends and family may pick sides. The kids may rebel. You may have to sell the family home and move to another. The financial situation may become difficult before it gets better. You may need to find another job.

With this many changes happening at once, it can’t help but create a change in you. The roller coaster ride through those changes, and where you land when it is over, will be your transitional journey. And on that journey, you will experience a flood of emotions.

It’s no wonder why major life changes are stressful. Reducing your stress in any way possible will make coping with life changes and transitions much easier.

When you breathe deeply, take a run or kick-box, meditate or get a massage, you can activate the hormones in your body that lower your stress level. Find the right way for you.

Some stress is good. It can be a motivator. But too much stress can hold you hostage and keep you stuck in a place that you don’t want to hang out.

3. Embrace What You’re Feeling.

Now, that’s an odd way to put it! How do you embrace something that doesn’t feel good to you? Like fear, uncertainty, grief or anxiety. I say “embrace” it because that is what allows you to take some control of it, rather than allowing the emotion to control you. It offers you a different perspective on emotion.

Take fear for instance. The feelings you might experience from fear are a pit in your stomach, shaking, sweating or unable to think clearly, to name a few.

What if you reframed the fear? Instead of feeling fearful, call those feelings excitement. When you are excited you may also have a pit in your stomach, shake at the knees and have sweaty palms. Embrace the feeling and call it something that empowers you. It’s a mindset shift.

You can do this with many emotions. I often think about grief as love that has nowhere to go—so I channel the love in another direction. It makes me feel better.

4. Plan for What Might Happen.

Although there is only so much you can control when it comes to life change, there is some benefit in planning for change that is inevitable. You may not know the exact timing or scenario, but you can pretty much count on things changing at the most inopportune moments. That’s how life works.

Feeling prepared can lower your stress and keep your emotions in check. Creating a checklist of things you want to do when something major happens can help you and help those who are there to help you through whatever the event may be.

Here are some ideas to get you started:

  • Develop a “things to know should something happen to me” document. Include all the important account numbers, links, and passwords so your designated person can pay your bills or call your friends and family.
  • Make a list of the things you would want someone to bring you should you be hospitalized.
  • Make a list of everything you would want to take out of your house in case of an emergency and you couldn’t get back in for a while.

I don’t suggest you start thinking about all the worst-case scenarios and dwell on them. Just make the lists and be prepared. Peace of mind is the goal.

5. Give Yourself Time to Rest.

Rest your mind. When coping with life changes and transitions, taking a break is important. Stop thinking so much. Turn down the volume of your self-talk, especially the negative thoughts that can swirl around in your head.

What is your favorite way to “veg-out?” Binge watch a favorite program that takes your mind off what you’re going through.

Play a mindless game on your smart device until you realize you’ve spent an hour not thinking about the situation that weighs heavy on your heart right now.

Play with your pets. Take an amazing walk in nature and focus on how gorgeous it is. Sit by the ocean or a babbling brook and listen to nothing but the sounds you hear. Put earphones on and sit quietly with a guided meditation.

Taking mini-breaks does your mind, heart, and soul a lot of good when practiced at regular intervals.

6. Learn How to Be More Resilient.

Bouncing back from adversity when you are coping with life changes and transitions isn’t easy, or for the faint of heart.

One way that can help is to think back to times in your past when you have bounced back successfully. What did you do then that you can apply to what is going on now? Which lesson that you learned could be put into practice to make this time easier?

Think hard about those times. When you flex that muscle again, it will build your resilience and uplevel your confidence that you can make it through this life change.

7. Don’t Neglect Self-Care.

There are so many benefits of self-care. Especially when life turns you upside down, the best way to turn yourself right side up again is by taking care of you.

Building resilience so you can handle major life changes and transitions is an important part of the equation.

Feeling strong and capable comes with getting enough rest, eating well, and moving your body so it feels good. Relaxing in ways that feed your soul with massage, swimming, or gardening, begins to fill your cup.

Think of a beautiful teacup and saucer. When you have replenished your cup, and keep it full to overflowing by taking care of yourself first, then you can give from the overflow.

With a full cup, your stress level is managed, it’s harder to get you rattled, and you can make better decisions.

Take care of you first! It will help a lot when you are coping with life changes and transitions.

6 Things We Do Instead of Expressing Our Real Emotions (and How It Affects Our Health)

8. Ask for Help When You Need It.

Being a lone wolf, withdrawing from your life, or struggling to figure things out can make your head hurt. And it can keep your heart feeling heavy. Share your burden with others you trust and lighten your load.

When it comes time to take control of your situation and move forward, think of yourself as the “chairperson” of your life.

Every great chair needs a board of directors. These are people who will lift you up and encourage you. They will be good at things that you’re not expert in. Choose people who can fill roles that support you at this point on your journey — you can add other people when things shift for you.

Who can you ask to be a member of your board?

Each of these strategies can add powerful tools to your treasure chest. They are ones you can adapt to your own situation while you are coping with life changes and transitions.

Once you’ve adapted them, you get to apply them and practice them until you have created new habits and integrated these strategies into your life. They become tools in your treasure chest forever that build resilience.

This guest article was originally published at Life Care Wellness and appeared on YourTango.com: 8 Easy Ways You Can Embrace Change Without All The Stress & Anxiety.

from World of Psychology https://ift.tt/2Qj1wkc
via theshiningmind.com
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Advice for Parents of High Functioning Autistic Children from Someone Who’s Been There

When raising an autistic child, doctors and therapists come in handy in answering questions that parents of autistic children may have. God knows, we’ve consulted our share of specialists. But sometimes, no advice compares to the advice of the very people who are raising these children. My husband and I have been in the position of bringing up a child on the spectrum for 15 years.  We’ve seen and learned a lot, and I’d like to share some of the tips we’ve learned over the years.

Know That Sometimes It Takes Years to Get a Diagnosis

Many autistic children are diagnosed at a young age, but for some, it takes a while. We suspected something was different about our son when he was very young. He wasn’t talking at around two, so we got him a speech therapist. Then, when he was four, we had him evaluated — no autism diagnosis. We had him evaluated again when he was about seven — again, no diagnosis. It wasn’t until he was ten that he was diagnosed.

The lesson here is if you suspect autism, keep up the evaluations. Ironically, things can become easier with a diagnosis; you can receive more services and accommodations. Life is less confusing, when you know what’s wrong and can get the appropriate help your child needs.

Realize that Things Change

Autistic children, like typical children, aren’t static. Kids grow; behaviors change; new knowledge is gained; empathy and social skills are learned. For instance, my son had behavioral issues when he was a young child, but as he became more verbal and less frustrated socially (he learned to make friends), these behavioral problems diminished.

Enlist Your Friends to Help You with Your Child (It Takes a Village)

Many of your friends have special talents that they can share with your child. Ask them to get on board and share some of their skills with him or her. For example, our son loves art. He loves to draw and create cartoons. We employed our friend Rachel who has a degree in art to work with our son during the summer months. They did many fun projects such as making a sculpture of a mushroom. (My son was investigating mushrooms at that time; as you know your autistic son or daughter may become fixated on the oddest things.) Rachel and our son met for a couple of hours on Wednesdays. Their interchange was invaluable. Our son learned more art skills, but he also developed his conversation skills as well.

Be Open to Difficult Questions

“Mommy, am I disabled?” My son began asking this question at 14. For about a month, I avoided answering it. But when I answered openly that he did have a mild disability, the air was cleared, and he began to relax about his identity. Other difficult questions might be, “Will I get married and have children?” The bottom line is you need to address questions such as these even if you relay that no one can tell the future and that you certainly hope his adulthood will be exactly how he wants it to be.

Watch Out for “Snake Oil Salespeople”

Everyone and their brother seem to have answers for how to treat and even cure autism. But watch out; some people exploit vulnerable parents of autistic children, charging them exorbitant amounts of money and offering them quackery. My husband and I have run into a few of these types of people; one woman wanted to sell us a sound system that would “rewire our son’s brain.” Just remember, if the promises for success seem too good to be true, they probably are.

Talk to Other Parents of Children with Autism

Take advantage of those who have navigated the system before you.  

We have good friends who have a child on the spectrum. I always consult with them because their daughter has participated in programs that have been successful, and they can recommend our next steps to be taken. For instance, their daughter did a wonderful job training program for special needs children. When our son was ready to start thinking about being employed, I signed him up for this very program. Other parents have had successes and failures on their journeys with their children. Mine their experiences.

Take Advantage of Interests and Abilities to Boost Your Child’s Self Esteem

Autistic children have strengths and weaknesses just like typical children. It’s beneficial to discover what your child is good at and encourage him or her to engage in this activity. When your child is successful at hobbies or interests, it boosts their self-esteem.  

For example, our son loves running, improvisation and bowling.  We are sure to involve him in these activities on a weekly basis. This helps him become his best self.

Don’t Talk Down to Your Child

If you want to encourage maturity in your autistic child, don’t talk down to him or her. Sometimes this is hard to remember, but the most successful parents of autistic kids talk to them and treat them as “normally” as possible. Here’s an example: I try to use my full vocabulary with my son, and consequently, his language skills are now getting fairly sophisticated. Remember, avoid baby talk. 

Living and thriving with an autistic child or children is not easy. But it is doable. You will accomplish your goals by relying on specialists to guide you, but don’t forget the laypeople in your life that live day in and day out with those on the spectrum.  

I wish you luck on your journey. Trust your instincts. You know your child better than anyone.

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via theshiningmind.com
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Podcast: Parents of Children With Mental Illness



Chrisa Hickey’s journey into mental health advocacy started when her son, Tim, was diagnosed with very early onset schizophrenia after being admitted to a psychiatric hospital for the first time at the age of 11.  He had been showing symptoms for years and had received a half dozen different diagnoses. His family was desperately looking for answers.

Tim’s illness took a toll on the entire family, which was only exacerbated by the lack of information and resources available to them.  In America, fewer than 100 children per year are diagnosed with very early onset schizophrenia. Chrisa had to find information and resources for herself and didn’t want anyone else to have to start from scratch.  And so the Parents Like Us Club was born.

Join Gabe and Chrisa as they talk about the struggles of dealing with a mentally ill loved one, especially a child.  And find out what has helped Tim, now 25, achieve the happiness and stability he has today.

SUBSCRIBE & REVIEW

Guest information for ‘Parents Mental Illness’ Podcast Episode

In 2009, Chrisa Hickey began writing a blog about raising her son Timothy, diagnosed at age 11 with childhood onset schizophrenia. Marian, one of her readers (who later became a friend) commented that parents raising children with severe mental illnesses were sort of a strange little club, and that there were other “parents like us” that should be part of the club. In 2015, the club was formed. Chrisa began collecting stories of other Parents Like Us and posting them to her blog, www.themindstorm.net. But this didn’t seem like enough.

In 2019 Parents Like Us Club Inc. became a 501©3 charity with the mission of bringing together parents raising children diagnosed with schizophrenia, bipolar disorder, major depression, and other life-threatening mental illnesses and serving three roles for this community:

  • Give voice to families raising children with severe mental illnesses by sharing their stories with other parents, the public, and the medical community
  • Provide resources and information for parents so that no parent has to try and figure out the complex maze of educating, treating, and caring for a mentally ill child on their own
  • Give parents the extra support they need by funding in-person advocacy services to attend school meetings, doctors appointments, meetings with social services, and judicial processes with parents, to help them navigate the complex issues that surround raising our kids

About The Psych Central Podcast Host

Gabe Howard is an award-winning writer and speaker who lives with bipolar disorder. He is the author of the popular book, Mental Illness is an Asshole and other Observations, available from Amazon; signed copies are also available directly from Gabe Howard. To learn more, please visit his website, gabehoward.com.

Computer Generated Transcript for ‘Parents Mental Illness’ Episode

Editor’s Note: Please be mindful that this transcript has been computer generated and therefore may contain inaccuracies and grammar errors. Thank you.

Announcer: Welcome to the Psych Central Podcast, where each episode features guest experts discussing psychology and mental health in everyday plain language. Here’s your host, Gabe Howard.

Gabe Howard: Hello, everyone, and welcome to this week’s episode of the Psych Central Podcast. And today, I will be speaking with Chrisa Hickey, who is the mom of a young man with schizophrenia and an incredible mental health advocate. I’m proud to say that I’ve worked with Chrisa in real life and she is doing incredible work. Chrisa, welcome to the show.

Chrisa Hickey: Thank you, Gabe. How are you doing?

Gabe Howard: I am doing very well. You know, we’re both mental health advocates, so that’s just generic. We can get that right out of the way and nobody knows what that means. But as longtime listeners know, I live with bipolar disorder. So I always do my speaking from the lived experience, what it’s like to live with mental illness. And why I’m so drawn to you and why I like talking to you and learning from you is your lived experience, and the majority of your advocacy is from the, you know, I hate to say caregiver, but from the family member, from the mom who is advocating for her son. Can you can you kind of give us that story?

Chrisa Hickey: Sure, a lot like your story, I’m sure no one gets it, wakes up one morning, goes, I want to be a mental health advocate. For us, it started when my son, Tim, who will be 25 in a week or so now, was four years old. We knew that there was something going on with him. We just weren’t quite sure what it was. And we started going through with doctors and neurologists and neuropsychologists and therapists and everything else. Long story short, after several different diagnoses and all kinds of issues, he ended up on his first psychiatric inpatient stay at the age of 11 when he attempted suicide. And doctors there said, well, what no one wants to tell you is that your son has schizophrenia. And I said, no, he doesn’t. Because kids don’t have it. And I didn’t believe it. And then six months later, he tried to kill himself again. And I went, OK. Obviously, you have a problem here. So at that point, the advocacy was personal. It became “what do I need to do to make sure that my child is getting the best care possible?” And I can try and give him a life and adult life. Because at this point, you know, you worry about whether or not your kid is even going to make it to adulthood. So that kind of morphed into all kinds of things you do when you have a child, especially with a serious mental illness. It really does become a family disease. Everyone’s affected. Parents are affected. Siblings are very affected. Everyone’s affected. So when I started doing my advocacy work on that, I found other parents who were struggling with the same kind of things we were trying to figure out. I started sharing information and started my blog and getting people to help share their stories. And we basically built this. I ended up building this community of parents who were all trying to help each other because not even our clinicians really could help us very well because it’s pretty rare. I mean, there’s about 100 children in the US every year, diagnosed with childhood schizophrenia. So we’re a small fraternity.

Gabe Howard: That is very small. Even if we go with every single child who’s diagnosed with mental illness, that number is very small. It’s bigger than the hundred, but it’s still very small. And of course, we’ve all heard it said a thousand times in the mental health community, mental illness is not a casserole disease. When people hear about stuff like this, they avoid it. And here’s the question that I want to ask specifically, because I hear this all the time, and I do not have children and I am not a mom. But did people in your community blame your son’s illness on you? Because you always hear that society blames moms for mental illness.

Chrisa Hickey: Yeah. Well, for us, it’s a little bit different because Timothy is also adopted. So a lot of what we got was, and no joke, people would say, well, this is obviously because he’s a product, you know, of his birth parents. Why don’t you just return him?

Gabe Howard: Wait, what?

Chrisa Hickey: Yes. He’s not a toaster. It’s not like, you know, gee, this toaster is not toasting right anymore. I’m going to take it back to the manufacturer. People would literally say to us, because he was adopted, obviously, it’s not our fault. It’s something weirdly genetic with his birth parents or his background and whatever. Maybe we should just go and, you know, not get a kid that was so complicated.

Gabe Howard: Wow.

Chrisa Hickey: Which just stunned me. Yeah, it totally stunned me. But I’ll tell you what really did happen with neighbors and people at school and stuff. What they wanted was their kids to stay away from him because they were worried that he was he was dangerous or erratic. And that’s the thing. Whenever you hear about schizophrenia, your mind always goes to — insert horror movie here. So, you know, you get little kids were like, oh, my God, he’s got this terrible disease or a split personality thing. Half the world still thinks that’s what it is. You know, we need to keep our kid away from him.

Gabe Howard: And it’s hard for children anyway because anything that makes a child different —  bullying is a real thing and cliques form and — but now your son is in a position where he could definitely use support and use friends and use understanding. But of course, he’s not getting it because kids are being children. But then there’s another layer. Parents are influencing their children’s behavior. And I just I struggle with that idea so much that a parent would tell their children, don’t play with another child because they’re sick. That’s just so scary.

Chrisa Hickey: That’s the problem, though. They don’t see him as sick, what they see it as, and this is why a lot of parents get blamed, they see it as a personality defect, right? Or a behavioral defect. It’s like the kid is not spoiled. He’s got an illness. But, you know, and I don’t know if you know this, but when NAMI was originally founded, it was founded by a group of parents — moms in particular — who were tired of being blamed for their children’s schizophrenia.

Gabe Howard: Yep. “NAMI Mommies.”

Chrisa Hickey: Yep. So that’s how it got started, and it would be great to say that there had been progress since they started this in the early 70s, but there has been very minimal progress. And it’s not just the public. The worst thing we fight against as well is a lot of clinicians don’t understand it, especially in children, because there is such a behavioral component. You know, it’s so hard to diagnose a child because when my child throws a temper tantrum, is it because he’s trying not to listen to the voices in his head or is it because he’s frustrated or is it because he’s a kid?

Gabe Howard: How did you as a mom, decide? When the tantrum occurred, how did you personally make that determination?

Chrisa Hickey: It was difficult to tell. And because it was difficult to tell, we started treating them all the same. The one thing with him it was easy to figure out was if he would escalate quickly, it probably was because of his illness. If he was just mad because we weren’t having Spaghetti O’s for dinner, that was something easily diffused and he wouldn’t escalate. It would be easy to talk him down. So I would start talking to him slowly, trying to understand what was going on in his head. And if it kept on escalating, then I knew that we had a real problem we had to deal with. But initially you don’t. Especially with the kids, you have to start treating them all the same, and that’s the hard part. Especially, imagine it happens in the grocery store. How do you explain this to people while you’re sitting there saying, OK, let’s sit down and calm and talk about what’s going on? And everyone’s looking at you like you’re crazy.

Gabe Howard: Right. So to take a step back. You said that you could tell something was wrong as early as four, but that he wasn’t diagnosed until he was nine. Is that correct?

Chrisa Hickey: Well, his first diagnosis was at the age of four. And at that point, they didn’t know whether it was an autism spectrum disorder or an emotional disorder. So he basically had this diagnosis called PDD-NOS, which is pervasive developmental disorder not otherwise specified. And from there he transitioned through several. So then it went to OK, it’s definitely not autism. This is emotional. So now it’s emotional disorder not otherwise specified. And then maybe it’s bipolar disorder or maybe it’s bipolar disorder I, or maybe it’s II, or maybe it’s bipolar with psychosis, blah, blah, kind of kept going, you know. When they finally said it was a schizophrenia, it was a doctor who had been consulting with the therapist. And the therapist had been reticent to tell us that she was positive it was schizophrenia. And he just basically blurted it out.

Gabe Howard: Wow. What were the specifics? What were you witnessing? What was your son doing?

Chrisa Hickey: He had a couple different things that were pretty routine, so he had some, which now we know are delusions, of course. Now there’s a clinical term, we call them delusions. But he had some weird idiosyncrasies, like he couldn’t put water on his face because something horrible was going to happen to his face, I don’t know, was going to melt him or whatever. But you could never put water on his face. He would have conversations with nobody. And I’m talking long, complex conversations with people. Like when I’m driving and he’s sitting behind me and the hair on the back of my neck stands up because he’s having a huge hairy conversation when no one is there. He had very little outward emotion. He wasn’t very happy. He was never very sad. He was just kind of flat. Right? So now we know clinically they call that “flat affect.” And when he had anxiety about all of this going on, he had some incredible rage. My husband and I were actually trained when he was eight years old in how to do a therapeutic hold because he was so strong. Well, here’s an example: at the age of eight, he took one of those kid desks with a chair attached to it and the lid lifts up, picked it up over his head and threw it at a teacher.

Gabe Howard: Oh, wow.

Chrisa Hickey: So he was pretty strong. So we actually were trained by clinicians on how to do a therapeutic hold, because if we didn’t, he could literally hurt himself or one of us. The rage was the hardest part to deal with.

Gabe Howard: So now you’re faced with all of this. You got the doctors, you do all the right things. You’re advocating for your son. We could probably talk for hours upon hours how difficult it is to find the right care, the right treatment, the right clinicians. But moving all of that aside, let’s talk about medication. Did you choose to medicate your child? Because it’s debated a lot.

Chrisa Hickey: It is. So initially we didn’t want to medicate our child because the last thing you want to do is — and it’s the prevailing thought out there, right — I don’t want to put this poison into my kid. But it got to the point where after several hospitalizations. I mean, he had 16 hospitalizations between ages of 11 and 14. So you get through the first three or four hospitalizations, you finally realize that you can’t do this just with behavioral intervention alone. You know, we didn’t want to put the poison in Tim. So we started very slowly and we wanted to start with — does he need a mood stabilizer? Does he need an antipsychotic? And we start working with the doctors to try and create whatever the cocktail is. That’s right. But every time you put these pills into your kid, a little part of you dies inside because you’re thinking — and I hear this a lot from other parents — the number one thing they say is when they have to give their kid meds or put their kid in the hospital, is that they failed as a parent. It’s self stigma.

Chrisa Hickey: And that’s the hardest part. And it’s a cliche. And we all say it’s like if your kid had diabetes, you wouldn’t feel that giving him insulin. But it’s really true. My kid has a brain disorder, not a brat, not a behavioral issue. He has an illness in his brain. And if I can give him medication that helps that illness in his brain, let him live the life that is most fulfilling as possible, then that’s what we decided we had to do. I think the hardest part for parents with kids, though, is unlike adults, kids change a lot. They grow. And as he would grow and get older, we would feel OK, we’ve put him on meds and he’s doing stable. And then six months later he’d have a growth spurt and everything’s out the window. So we’d start the whole process over again. And so every time he would go onto meds, it would change or something, we would all brace ourselves because we didn’t know what was coming. Most parents don’t want to medicate their kids. Kids are getting stigmatized for taking the meds they really need.

Gabe Howard: Again, I’ve never been a parent, but I can talk about my personal experience when they were like, hey, you have to take meds in order to be human. I’m like, you know, I’m 25 years old. I’m a grown ass man. I don’t need this. I’m fine. I’m fine. I’m fine. You know, I was very much in the I’m not sick. My mom is good. So therefore, I can’t be mentally ill. Plus, I have a personality and a job. So, sickness is for other people and other families and other problems. The medication was, you know, pardon the pun, a tough pill to swallow. And that was in me. And I’m making the decision for me.

Chrisa Hickey: Can I ask you a question about that, though? Is that because you saw the medication as because of your personal failing? Because I think it’s so ingrained in our society that mental illness is because we’re weak or we’re spoiled or not parented well, or we’ve got a personality defect that even to ourselves, when you are telling me I have to take a pill so I can act and feel normal, we feel like failures.

Gabe Howard: Yes. And it’s a little deeper than that. One, it was a reminder that this is the suckiest part about being on medication. You know, picture it: twenty five year old Gabe. I’m still that age where I think that I’m invincible. And of course, I have bipolar disorder. So I go through mania which tells me that I am, in fact, not only invincible, but God, because that’s what mania is like. And every morning and every night, I have to take a handful of reminders that I’m weak. That is 100 percent true. That is a demarcation twice a day that I am different from my peers. Now I’ll add on to that that my peers, you know, they’re good people. I have no negative stories of my friends being mean to me on purpose. They would all make little jokes. All there is Gabe with his granny pill minder. Oh, Gabe’s got to go to the pharmacy with all the grannies. They thought they were being friendly and ribbing me about it. It hurt and it hurt in a way that I couldn’t explain. I couldn’t put my finger on it. We’ll be back after this message from our sponsor.

Announcer: This episode is sponsored by BetterHelp.com. Secure, convenient, and affordable online counseling. Our counselors are licensed, accredited professionals. Anything you share is confidential. Schedule secure video or phone sessions, plus chat and text with your therapist whenever you feel it’s needed. A month of online therapy often costs less than a single traditional face to face session. Go to BetterHelp.com/PsychCentral and experience seven days of free therapy to see if online counseling is right for you. BetterHelp.com/PsychCentral.

Gabe Howard: We’re back with Chrisa Hickey, founder of the nonprofit ParentsLikeUs.Club.

Chrisa Hickey: I have said to people before, and people look at me like I’m wack when I say this, but I do feel like we’re really lucky that Tim was diagnosed so young because when Tim was eleven, he didn’t get a choice whether he took his meds or not. He didn’t get a choice if he went to his doctor or not. He didn’t get a choice if he went to therapy or not. He did it because he was 11 and I’m the parent. So by the time he was 18 or 19, it was such a routine for him, he didn’t think about it.

Gabe Howard: And this is an incredible point to bring up because you’re absolutely right. I was 25 years old when I was diagnosed and I had a choice.

Chrisa Hickey: You have a parent who also has a mental illness or you have a parent who doesn’t understand it and is still trapped in that kind of stigma and blame cycle. The number one reason kids who die by suicide. I mean, children who die by suicide die because they weren’t in treatment. And the reason they weren’t in treatment is because their families didn’t want to believe there was something wrong with them.

Gabe Howard: And why do you think that is?

Chrisa Hickey: So I just think that when parents think a kid is depressed, I don’t think they understand. Suicide kills more kids than anything in the world except car accidents. I mean, it kills more kids than cancer and every birth defects combined. Suicide, depression. There’s “little d” depression like, you know, oh, my friends never call me, I’m so depressed. And then there’s “big D” Depression, which is clinical. And with all the stresses that kids are under now about, you know, achieving and getting into good schools and scholarships and student loans cost so much. And what am I going to do? That when a kid shows something that actually looks like clinical depression, they don’t want to believe it because if they believe it then that whole belief about what your child’s life was going to be, it’s shattered. You know, it’s something a lot of us parents have to go through if we have a kid with a mental illness. You actually go through a mourning period when you actually accept the fact that your child has a mental illness. That what I expected my kid to grow up to be and have for his own life is gone. When Tim was little, he was a gorgeous child. He loved to sing with the radio and everything. He talked about wanting to be a pilot. All kinds of stuff, you know. And when they told us he had schizophrenia and it really digested, it’s just you could almost hear the glass shatter and you go through an actual mourning period where you’re mourning someone who’s still alive. And you end up doing it more than once as you go through this whole cycle. And I think a lot of it is because these parents don’t want to have to think about what happens if.

Gabe Howard: Because it’s scary and they don’t have anybody to talk to. Which is what you learned early on. You couldn’t just reach out to the other moms and dads and say, hey, I’m toilet training and it’s a nightmare. These are the things that parents do. These are the things that people do. We reach out to like minded people to share stories and get advice. But you didn’t have anybody to reach out to. And that was why you started blogging and that’s why you built a community. And that’s why you launched ParentsLikeUs.club, which I didn’t even know .club was a domain address.

Chrisa Hickey: It is. Isn’t that cool? Yeah. Well, you know, when I started the blog and other parents were sharing their stories and I started sharing them on my blog as well. One of the moms there said, this is like a club. All these parents like us. We’re like this big club. And I’m like, Bing. There we go. This is what we are, we are this sad little club. So we kind of formalized the name. And I had a section of my website just for the Parents Like US Club, where people can share their own stories anonymously or not anonymously. It is totally up to them. And then over the years, a friend wanted to start a support group on Facebook. So I helped her with that. We have a support group, a closed support group on Facebook that has now over almost ten thousand parents in it with all different kinds of brain disorders, not just mental illness, but kids with autism and other things as well. We wanted to formalize it, help people even more. You know, navigating medical staff and the job stuff when you’re an adult is one thing. Now you’ve got a kid. You’ve got to navigate school and you’ve got to navigate doctors and you’ve got to navigate a lot of times the criminal justice system. How do you navigate these things and how can we help parents that don’t know where to start? So we formed the 501©f(3) charity, Parents Like Us Club and we’re doing three things. We’re giving a platform for parents to be able to share stories. However they want to share. Video, they can give us blog post, they can do an audio. Be anonymous, not be anonymous, whatever.

Chrisa Hickey: Because we know and you know, as we share our stories, it’s important for the public, other parents, and especially for us clinicians to hear these stories and understand what families are living through. The second one is to give find resources for parents, because the reason I started my blog was I had to do research from scratch and I didn’t want anyone else to have to do research from scratch when you’re dealing with that. So how can we get all the resources out there? So they’re available and they’re indexed and you can find them when you Google it, you can find us and we can get different clinicians and people to actually go into a directory and tell us they actually specialize in helping kids. And the third thing is we’re going to be giving micro grants to families that need them to have professional advocacy work with them locally when they go to an IEP meeting at school or they’re going to see a new psychiatrist for the first time, or they have to go down and sit down with a lawyer and talk about the juvenile justice system because, A, it helps to have a neutral third party that is really an expert to take that emotion out of it and really understand what your rights are and your child’s rights are, and B, what’s the best course of action for your kid and what you want to get out of them. So those are the three things we’re trying to accomplish, but we’re [unintelligible] this year, so we’re just getting off the ground.

Gabe Howard: I think it’s absolutely incredible. You know, when I was diagnosed, again, I was 25 years old and my parents and my grandparents reached out to meet other families, other family members who had, you know, family members who had mental illness, who had, in my case, bipolar disorder. And again, I wasn’t a child. You’re actually right. It’s you know, my parents were scared. My grandparents were scared. My family was scared. And they reached out to get that help. And I’m so thankful that they were able to find it. They’re in a big city. And there was support groups for this. The thing I like about your organization is it’s on the Internet. Like my parents aren’t shy. My grandparents weren’t shy. They started calling emergency rooms and therapists that, like where’s a group? We’re willing to get in our car and drive. But I talked to so many people that are like, oh, we’re not going to go to that support group meeting. We’re not going to walk in there. Somebody might see us. Or they’re in a small town. I don’t want to say that is your support group anonymous or is your club anonymous? But there is a certain layer of anonymity to it because it’s online. Or can you sort of talk about that a little bit?

Chrisa Hickey: There is and you know, obviously there’s always the option to be anonymous when you’re online. I think what a lot of parents do is, you know, you think about and again, it all kind of comes back to that stigma we’re all ingrained with. The worst part, I think for kids, too, is a lot of clinicians fall into the stigma category. So it’s like the reason Tim’s therapist was timid diagnosing him as schizophrenic is because they didn’t want to put it on the chart. You know, it’s on their permanent record kind of thing, whereas I’m like, you know, like I care. But a lot of parents are worried about that. They’re like, you know, I don’t want to hurt my kids’ chances to get to college. Maybe you work at a job one day, so I don’t want to put their name on the Internet and associate it with a mental illness. That’s fine. You don’t have to. But the nice thing about it being online is we talk about kids with serious mental illness and we talk about serious. We classify that as schizophrenia, schizoaffective disorder, bipolar disorder and severe clinical depression. So those are the diseases for kids that become fatal, frankly, as far as mental illness goes. If you take a look at the pool of people in the United States, just because that’s where I know best, if you’re talking about schizophrenia, 100 kids a year get diagnosed.

Chrisa Hickey: Small pool. Bipolar disorder, I or II or other type for kids, becoming less common because now there’s other DSM 5 things for it. But you get about two to three thousand kids a year get diagnosed with that. Severe depression, much more at 10 to 15 thousand kids a year, kids with severe depression. And that’s every year. So you’re talking, I don’t know, 20,000 people that need to find each other in the three hundred and fifty million people in America. I don’t have a choice but to go to the Internet. I mean, if I was back in the days, you know, when the NAMI moms were all starting to get together. I would’ve been screwed. My son, we lived in Chicago, not a small town. When my son was diagnosed and his psychiatrist, who was the head of child psychiatry for one of the largest mental health groups in Chicago, said Tim was the most severe case he’d ever seen. And he was 65 years old. And all I could think of was first my thought was, oh, great, my kid is, like you said, some sort of record for being whacked. But then the other thing I thought was how few and far between is it that my kid is the only one this guy in the second largest city in the country has ever seen?

Gabe Howard: And how lucky are you? You know, that’s the thing that goes through my mind. How lucky are you that you live in Chicago? Could you imagine if you lived in rural Ohio or or just anyplace rural?

Chrisa Hickey: Where we live now. Yeah. Now we live in rural Wisconsin. Yeah.

Gabe Howard: Yeah. Is there and I don’t mean this in any insult to anybody that lives in rural America, but there’s not gigantic hospitals in rural areas. There’s just not enough people.

Chrisa Hickey: No. So now I live in very northeastern Wisconsin, very, I mean, my town is 300 people. So if we had lived here when he was 11 and he was, we had to figure out what’s going on with him at that age. I would have had to go to Madison, Wisconsin, which is four and a half hours away, to even get come close to finding a clinician. And then when I got to Madison, the average wait in Madison right now for a first appointment with a child psychiatrist is 17 weeks.

Gabe Howard: 17 weeks, and we’re hearing that all of the time. This isn’t new news to anybody who’s done even the most basic mental health advocacy, that the wait times to see professionals are there so long. They’re insane. They’re insane.

Chrisa Hickey: They’re terrible. You know, a child psychiatrist is even rarer than a psychiatrist. So because it takes more schooling, right? If I go to school and go to medical school and become a doctor and then I go to my specialty and I become a psychiatrist to become a child psychiatrist, I’ve invested in even more time. And it’s not like they’re gonna make any more money being a child psychiatrist. So there’s really no incentive for them to do that. So there’s the shortage.

Gabe Howard: I am so glad that you were in a place where you could advocate for Tim. How is he doing now? You know, we’ve heard a lot about his childhood. I know that he’s almost 25 years old now. What is Tim’s adult life now?

Chrisa Hickey: It’s good. So we did move to rural Wisconsin. We moved back to the town my husband grew up in, actually, and the number one reason we moved here is because this is a much better environment for Tim than in Chicago. There’s too much stimulus in Chicago. There’s too many ways to get trouble in Chicago. And he’s very anonymous in Chicago. Here in this town, Tim is able to live in his own apartment because he only lives a mile away so we can help him when he needs help. He has a small part time job with a family friend who has resort cottages. So he’s got some sheltered work where if he’s having a bad day and he can’t show up, it’s no big deal. He can come to work everyday. And if he misses a day, no problem. He has friends here. We live right on Lake Michigan. He goes swimming in the lake in the summertime. And he has his own dog now and he has his bike and he rides all over town and everybody knows Tim. He really is a happy person. And he’s very, very stable. And a lot of the reason he’s stable is because he has an environment that supports him, because we’re in a small town where my husband grew up, we’re not anonymous here. It’s like having 200 extra hands to help watch him. Couple weeks ago, you probably know he messed up his meds a little bit, ended up in an emergency room. The paramedics all showed up when he had a problem with it because he lives across the street from the fire department. And, they know, know him personally. When he got to the emergency room, he knows the nurse there because she’s a neighbor. And, you know, when he was having an off day, I’ll get a phone call from one of his neighbors. You know, have you seen or talked to Tim today? He seems a little off. So we’ve created this environment for him where he’s very insulated. And I know that not only now at twenty five, but when he’s 55 and I’m no longer around, he’s still going to be safe and happy here.

Gabe Howard: Chrisa, this has been absolutely wonderful. Thank you for all that you do. Thank you for starting the nonprofit. And I don’t know if Tim has ever thanked you. But as somebody who lives with mental illness, you know, moms like you, parents like you, family members like you, they make such a big difference. It made a big difference in my recovery. And I know it made a big difference in Tim’s as well. So thank you so much for everything that you do.

Chrisa Hickey: Thank you. And thanks for having me. I really appreciate it.

Gabe Howard: Hey, it was my pleasure and thank you, everyone, for tuning in. Remember, you can get one week of free, convenient, affordable, private online counseling anytime, anywhere, just by visiting BetterHelp.com/PsychCentral. We will see everybody next week.

Announcer: You’ve been listening to the Psych Central Podcast. Previous episodes can be found at PsychCentral.com/show or on your favorite podcast player. To learn more about our host, Gabe Howard, please visit his website at GabeHoward.com. PsychCentral.com is the internet’s oldest and largest independent mental health website run by mental health professionals. Overseen by Dr. John Grohol, PsychCentral.com offers trusted resources and quizzes to help answer your questions about mental health, personality, psychotherapy, and more. Please visit us today at PsychCentral.com. If you have feedback about the show, please email show@PsychCentral.com. Thank you for listening and please share widely.

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Inside Schizophrenia: Working With Schizophrenia

Everyone complains about work. Having to go to work every day, working too much, not getting paid enough- working can be challenging for so many reasons. Today’s episode focuses on working while having schizophrenia. 

Host Rachel Star Withers, a diagnosed schizophrenic, and co-host Gabe Howard share antidotes from their own work lives and speak with fellow schizophrenic Michelle Hammer. Michelle, an award-winning graphic designer and entrepreneur, discusses her struggles working full time and transitioning to working for herself. Cheryl Wallace the Vice President of Programs at Rose Hill Center, a psychiatric treatment and rehabilitation center, also joins this episode and speaks about how Rose Hill facilitates programs to help people with schizophrenia rejoin the workforce after a psychotic episode. 

Highlights From “Working With Schizophrenia” Episode

[01:15] Rachel’s weird job history.

[03:00] Is it Rachel’s schizophrenia or her dislike for normal work?

[05:00] Being a stunt woman with schizophrenia.

[10:50] Guest interview with artist Michelle Hammer.

[13:43] Michelle’s family reacts to her decision to start her own business.

[16:13] Michelle’s advice to other people with schizophrenia who want to start a business.

[21:00] How Family and Friends can help.

[29:00] Reasonable Accommodations.

[34:00] Do you tell an employer you have schizophrenia?

[37:38] Guest interview with Cheryl Wallace the Vice President of Programs at Rose Hill Center

[46:34] It’s okay to work part-time, it’s okay to do what you need to do.

About Our Guests

Entrepreneur and Artist Michelle Hammer is an NYC native. She was diagnosed at 22 with schizophrenia. With her artistic talents and fearless personality, she founded Schizophrenic.NYC; a clothing line with the mission of reducing stigma by starting conversations about mental health. Schizophrenic.NYC takes a portion of the profits and donates to organizations in NYC that help out with the mentally ill population of NYC.

www.schizophrenic.nyc

 

 

Cheryl Wallace is the Vice President of Programs at Rose Hill Center. As one of the nation’s leading long-term mental health facilities, Rose Hill Center in Holly, Michigan offers comprehensive psychiatric treatment and residential rehabilitation services for adults, 18 and over, on 400 peaceful and serene acres. They offer effective therapeutic modalities including group and individual therapy and responsible medication management. Each week while living in on-campus townhomes, participants commit to 30 hours of meaningful activity. Some individuals will attend educational classes, find paid employment, or volunteer in the community.

www.rosehillcenter.org

Computer Generated Transcript for “Working With Schizophrenia” Episode

Announcer: Welcome to Inside Schizophrenia, a look into better understanding and living well with schizophrenia. Hosted by renowned advocate and influencer Rachel Star Withers and featuring Gabe Howard.

Rachel Star Withers: Listeners, could a change in your schizophrenia treatment plan make a difference for you? There are options out there you might not know about. Please visit oncemonthlydifference.com to find out more about the benefits of once monthly injections for adults with schizophrenia.

Rachel Star Withers: Welcome to Inside Schizophrenia. I am Rachel Star with my wonderful co-host here, Gabe Howard. Everyone complains about work going to having to go to work every day, working too much, not getting paid enough working can be challenging for so many reasons. But we’re going to explore working while having a serious mental health issue like schizophrenia. So I’ve done so many weird jobs, Gabe, like across the board. I was a wedding videographer for one day, one day and halfway through the day after the third bride came in complaining about their work. I was like, I I can’t do this. And I literally got up and left and I was like, you don’t have to pay me for today. I’m really sorry.

Gabe Howard: Do you feel that living with schizophrenia contributed to that because like you said, it’s boring, you’re sitting behind a monitor all day and then there’s confrontation, there’s chaos, and then there’s this whole, you know, wedding industry that we know about. Was all of that too much pressure? Because we know that you’re an accomplished video editor. There’s no question about that. What about this? Made it too much.

Rachel Star Withers: I think that it was such an open atmosphere like there. You could see everybody and you were sitting there nine to five video editing with all these people around. If I could have been sent the footage and done it at home, I probably would’ve been fine. But yeah, it was a lot and a lot of confrontation as far as people coming in. And weddings are boring.

Gabe Howard: So what other jobs have you had? I mean, we know about schizophrenic stunt girl, which we’ll get to at the end. What are some other just normal regular 9:00 to 5:00 jobs for Rachel Star?

Rachel Star Withers: Well, I haven’t had many 9 to 5 jobs, but of the ones I’ve had? One was I worked at a Christian furniture store in their marketing. And if you’re not from the south. Yes, that’s the thing. We have a lot of Christian stores like. That’s part of it. It’s in the logo is a giant cross.

Gabe Howard: Wow. Now, how long were you employed by the furniture store?

Rachel Star Withers: I was there for six months, which is like amazing for me to work or full time job for six months. And that killed me. I was oh, gosh, I mean, I. Towards the end, I eventually just went to one of the bosses, like, I can’t take this. I’m genuinely sorry. I guess I always feel so bad, like quitting something. I always apologize. Like, if I’m sorry, this place is horrible, but I’m sorry I led you to believe I’d be a good worker and I cannot take it here.

Gabe Howard: Just to be clear, do you think that it was because of living with schizophrenia that made you not be able to take it or was there something else going on or is it is it this kind of gray area where maybe it was a little bit of both? Is that hard to tease out?

Rachel Star Withers: I would say it’s absolutely a gray area. A major part was my schizophrenia. I have a very hard time doing the same thing day after day. I have a hard time doing the same thing for hours on end. About four hours in, I’m out. It’s just hard for me to pay attention. And that’s not like, oh, what about a lunch break mixes it up? Nope. If I’m stuck in the same place, it’s too much for me, and especially when it’s the situation of a desk. If I like literally stay in one place. Oh, I just go crazy. I can do it for about a few days. And then I start getting weird and I go downhill quick.

Gabe Howard: And I understand why you’re calling that a gray area because, for example, my father is a truck driver, my brother is an electrician. My brother in law is a police officer. And I point that out because none of them have schizophrenia and they all feel the exact same way that you do. They’re like, put me at a desk and that’s death. I don’t want to do it. That is horrible for them. They love doing stuff on their feet, working with their hands, moving around the city. I would hate all of those things. Like I don’t like to go outside. Now, I don’t want to be chained to a desk either, but I don’t want to do manual labor. So you learned that in your the beginning of their career. Sitting behind a desk bad. So then you started to get into some more like creative jobs. What were your jobs after the Christian furniture store?

Rachel Star Withers: Oh, I’ve bounced all over personal training. I’ve been a personal trainer. I’ve worked in gyms that’s always been like a kind of a side job for me. Every gym in the area here of Charlotte, I’ve worked in all of them.

Gabe Howard: Did you do better there?

Rachel Star Withers: So I’m totally fine if it’s a part time job or idealists say three times a week, they’re totally fine. I’m good with it. But if I have to go like day after day, I can’t take it. Even doing the same activity day after day, it just it wears on me and I get burnt out bizarrely quick.

Gabe Howard: And then you moved on from from personal training. You did what has really lasted the longest, right? The stunt woman. The modeling, the acting instructor. So you found your niche. And the reason that I bring that up is not because you’re really, really good at it, because you are really, really good at it, but because you went through a lot of different jobs to find the thing that work. Now, being a stuntwoman sounds really cool. But but from a job perspective, remove the cool and talk about that the day to day, the nuts and bolts. Why has this lasted? In a way that personal trainer at a gym or marketing at a furniture store or videographer for didn’t?

Rachel Star Withers: I started making stupid videos of myself after I got obsessed with Wild Boys, which was a spinoff of Jackass.

Gabe Howard: Jackass was a show where people filmed themselves doing stupid stunts or just doing stunts. I mean, we don’t even have to put stupid in front of it. Just just ridiculousness.

Rachel Star Withers: Yes. Things you shouldn’t do, things cmmon sense would say, “Don’t do that.”

Gabe Howard: And you did them and for example, like laying on a bed of nails, like walking across glass, you know, you’ve done some of these things and you still do them to this day and you excel at them and people enjoy watching them. And you you’ve made a career

Rachel Star Withers: Mm hmm.

Gabe Howard: Out of it.

Rachel Star Withers: Yeah. My thing was let’s see what’s possible and have fun, so it wasn’t so much like, oh my gosh, that’s so amazing you can do that. It was I show everything. I showed the complete fails. That’s usually what’s funny is the fact that I’m trying something that is clearly not going to work. But sometimes it does. And even I surprise myself. And you can probably tell by my voice, I’m more excited talking about that because it was something that was interesting to me and I was very lucky that I put it on the Internet and a TV show contacted me and I’d never realized, oh, I could make money at this because I was just being stupid of and that was like 14 years ago. And it kind of evolved into me going to full on stunt school to try and actually be in movies for it and different things. And, you know, as you do one thing, you learn others. And I learned about how to do all types of other entertainment similar to this podcasting.

Gabe Howard: But here’s something that I want to touch on for a moment, you know, I first met you at an event and you talked about setting yourself on fire and full disclosure. I met you as a woman living with schizophrenia. You talked about setting yourself on fire. And I immediately thought, OK, that’s not good. That sounds very bad. Now, you went on to explain that, hey, look, there’s a safety protocol. And I started thinking, I’m like, wow, that there are a lot of safety protocols now. Now, again, as somebody who lives with bipolar disorder, I would like to think that I’m above creating stigma or believing stereotypes. But but I’m not. I thought to myself, how does a woman living with schizophrenia set herself on fire and keep herself safe? Can you talk about that for a moment? Because if you don’t follow all of these safety protocols, you could get very hurt.

Rachel Star Withers: I have been hurt a few times, but it had nothing to do with my schizophrenia. Yeah, no, it’s funny because I started out doing crazy stunt videos and things. I didn’t talk about my schizophrenia. I didn’t open up publicly about it until years later. And I’ve always been very careful to not combine the two. It’s I’ve never made a video like, yo, I’m Rachel, I’m schizophrenic. Let me go run my head into a wall. Like, they’re very like I’ve always kept it separate because for me to safely do stunts and for one for them to be entertaining, I have to be all mentally here. So I can’t even film when I’m off. And when it comes to fire, I usually I have a spotter and whatnot and many times it’s my father. So like nothing bad could happen from, let’s say. Me not being fully there.

Gabe Howard: And you recognize that and make make good decisions that the people around you are also empowered to say, hey, maybe today is not the day.

Rachel Star Withers: Yeah, I’m never really filming alone, doing anything, there’s always someone there just as backup around, even on my little baby stunts. So yeah, the bigger the stunt, the more people actually have that have to help me with it.

Gabe Howard: I bring this up because a reasonable person hearing that somebody’s job was stunt person would think, OK, well, they have help. They have safety nets in place. They sometimes literally safety nets. But like you said, they’re not just running around with a camera doing these dangerous things all by themselves. But in your situation, also living with schizophrenia, you’ve also built up a safety net around not being off to make sure that you are mentally able to complete the stunt and relying on the people around you and yourself to know what that is. So again, that we get to the gray area, right, because living with schizophrenia is not the only types of people that have to be perfectly well to do stunts.

Rachel Star Withers: Right.

Gabe Howard: So being in control of these things and making sure keeps you and everybody else safe.

Rachel Star Withers: Right. And just distress. I have been trained, I have actually gone to stunt school. And yes, it’s not even just. Oh, well, I’m mentally sane, I can totally set myself on fire and watch this YouTube video on how to do it. Like, no, I have actually went to like a school for it and I’m constantly doing trainings and things to learn the correct way to do things. It’s just like getting a job. You have to be trained to do it.

Gabe Howard: Speaking of boring at 9 to 5 jobs. We got to interview Michelle Hammer. Now Michelle Hammer is the owner of Schizophrenic.NYC. It’s a clothing line that empowers people with mental illness to be their best self. She’s also going to talk about being a graphic designer in New York City who lost a number of jobs before she came to terms with what she could do and what she couldn’t do as far as being a person who lives with schizophrenia in the workplace.

Rachel Star Withers: I absolutely love Michelle and she has done so much. Let’s talk to her right now.

Rachel Star Withers: We’re here with our first guest, Michelle Hammer, who is an award winning graphic designer and an entrepreneur with her Web site being schizophrenic.NYC. Michelle, it might come as a shock, but you’re schizophrenic too, right?

Michelle Hammer: I believe so. I’ve been told that many, many times. I hope so.

Rachel Star Withers: So in your work career, you’ve actually worked for some pretty big design firms. What was that like?

Michelle Hammer: It can be very difficult because, you know, you work on your design and then you get asked to get approved by a million different people. And it’s just annoying and it’s frustrating. So I like to just not do that anymore.

Rachel Star Withers: What have you found to be the biggest challenges working for other businesses?

Michelle Hammer: Just dealing with the hierarchy of other people telling me what to do all the time, especially when you’re schizophrenic and you’re trying really hard to pay attention on what you’re doing and then people just keep giving you direction. And it’s just really confusing. Just cognitive skills aren’t that great, sometimes, you know, when you’re schizophrenic and you just try to understand as much as you can and you try your best. But sometimes it’s just really hard working for other people.

Rachel Star Withers: As far as with the schizophrenia, were you ever just kind of like unable to revise something?

Michelle Hammer: It’s not that I was unable to revise things. It was just frustrating a lot of times when you’re just hearing voices in your head or you’re just talking to delusions or hallucinations. It’s just there are really big distractions sometimes. You don’t really understand what people are really saying to you or you’re not understanding the direction or the rules or there are so many things on your plate. It’s hard to, you know, really understand like this. Do this here, do this here, do this here, do this here and just kind of try to problem solve your way through every single thing you have to do can be very, very challenging.

Rachel Star Withers: So you went from having what I would assume is some pretty coveted jobs for artists working for these firms to putting that aside and working for yourself. What was the biggest challenge in doing that switch? That’s hard for anybody, but especially when you have a mental disorder going on.

Michelle Hammer: Yes. So eventually I just I couldn’t work for anybody else anymore. It just wasn’t working out. I couldn’t do it. I can’t work. I can’t get in at 9 a.m. anymore. It was too much. I decided I’m going to work for myself. And that was interesting. I just kind of just went right into it and started just starting schizophrenic.NYC, my mental health clothing line. Just made some shirts and went to a pop up shop at the Long Island City Flea and was like, Hey, buy my shirts.

Gabe Howard: How long ago did you start schizophrenic.NYC?

Michelle Hammer: This is my fourth year, I started in May 2015.

Rachel Star Withers: When you first decide to do this, were your family and friends, like, really supportive or they were like, oh, Michelle, no?

Michelle Hammer: Oh, my goodness. It’s actually like my my mother contacted my doctor. I was like, what is she doing? Like, what is she spent a lot of money on these T-shirts? What is she doing? And even my doctor was like, are you sure you want to do this? Are you sure you want to tell everyone you have schizophrenia? Do you really want to do this? Is it something you’d really want to do? And I was like, yeah, I’ll do it. Yeah, yeah. I really want to do it. And everyone around me was like, are you are you sure? And I was like, yes, I want to do this.

Gabe Howard: Just to clarify, the issue wasn’t whether or not they felt you could start a business. The issue was whether or not you should boldly and loudly proclaim that you’re a person living with schizophrenia.

Michelle Hammer: Yeah.

Gabe Howard: So they had full faith in your ability to start and run a business. Even with your mental disorder, they just questioned the type of business.

Rachel Star Withers: From this, you know, you’ve branched off. I have some of your artwork where you can buy some of Michelle’s artwork at different things, but also the T-shirts, the different inspirations, kind of that you put out. The “Don’t be paranoid. You look great.” I love that. Where do you see the future of schizophrenic.NYC going?

Michelle Hammer: Oh, my goodness. The future of schizophrenic.NYC, who knows? We’ll see. We’ll see what’s happening. I’ve been working with a lot of advocacy, everything that’s going on right now with the gun violence and blaming the mentally ill. I had a protest in Union Square in New York City and we’re just trying to just keep going. Keep fighting the man and keep getting bigger and bigger and bigger. Have a new shirt that we came up with that says, “I am mentally ill and I don’t kill.” And we’ve gotten a ton of preorders on it and can’t wait till they’re ready for everyone to wear and everyone to just wear. A big sign that says that on their shirt, to start more conversations and to just start a whole movement of please stop blaming us, please.

Gabe Howard: I love how you frame that. And it’s also important to point out that you’ve really evolved past your stated goal of just being a graphic designer and selling shirts. You’ve branded yourself as a personality. You’re your own public relations firm and you really do a lot of work in a very high level.

Rachel Star Withers: Your advice to other people in our situation with a mental health disorder? Because I think you have the fear of one starting a business. But then the fear of what do I do if I can’t handle it? Sometimes I have like little mental attacks or I’m like, oh, my God, I don’t know if I can handle this. What is your biggest advice to people like us?

Michelle Hammer: Just go for it. Just try it. You can’t do anything. You don’t know if it’s gonna work or if it’s not going to work if you don’t try. Just try. I get messages all the time on my Instagram. Like, how can I start a business like you? How can I start something like this? And my answer always is. Hustle, hustle, hustle. Just hustle. I used to have a pop up shop where I started at 10 a.m. and then I would leave at 10 p.m. Twelve hours. Just hustle. Talked to as many people as I could talk to. Just sell for as long as I can. I was out there forever, just trying my hardest. Meeting as many people, talking to as many people. And I have great stories. I would meet people and I would tell them that I had schizophrenia and everyone that I would meet, they would either say they had a mental illness or friend of theirs op a family member of theirs does, or where they work in the mental health field. So it always baffles me why there is so much stigma around mental illness, especially in New York City, where one in five individuals has a mental illness. But nobody talks about it because of all the stigma. So really just trying to, you know, change the conversation. Change the conversation.

Gabe Howard: Is it fair to say that running a business is the same for somebody with schizophrenia as somebody without schizophrenia? There’s no magical difference in rules. I mean, business is business.

Michelle Hammer: Business is business and people are going to judge you differently. If you’re running a business with schizophrenia or not, they’re going to say it’s 10 times harder for you.

Gabe Howard: Is it 10 times harder for you?

Michelle Hammer: Well, I wouldn’t know because I’ve never run a business not being schizophrenic.

Gabe Howard: Excellent point. Thank you, Michelle.

Michelle Hammer: Yeah.

Rachel Star Withers: Michelle, do you have anything you want to promote specifically coming up?

Michelle Hammer: Not anything specifically coming up, but you can totally buy my stuff at schizophrenic.NYC and love everything. T-shirts, pillboxes, artwork, leggings and you know, I got tons of anything you desire.

Gabe Howard: Michelle designed the book cover for “Mental Illness Is an Asshole” as well. I mean, you do a lot of design work outside of your own advocacy work and your own brand as well. I mean, you’re quite prolific. Do you have a website for your graphic design work?

Michelle Hammer: Yes, it’s HammerTimeDesign.com.

Gabe Howard: I highly recommend.

Michelle Hammer: Yes.

Rachel Star Withers: That was great. I always love getting to talk to Michelle.

Gabe Howard: It’s interesting how, like, you both worked really, really hard to get to where you were. You both understood that you needed accommodations and coping mechanisms and you both, as we heard before the interview and then in Michelle interview, you both had a lot of jobs that you just had to quit or in Michelle case, get fired from before you realized what you could do versus what you couldn’t do. And then finally, you’re both so successful because you didn’t dwell on what you couldn’t do. You figured out what you could do and excelled at it.

Rachel Star Withers: And I love in Michelle’s interview where she actually says that the main secret to her doing this is hustling, you know, is if this is what you want to do. Fight for it. And that’s not, you know, great advice for someone with a mental health disorder. It’s great advice for anyone who wants to do something. Starting any sort of business is insanely hard. And to keep it alive for multiple years is amazing for anybody.

Gabe Howard: It is, and, truth be told, if we’re really being honest, holding down a 9 to 5 job Monday through Friday or whatever job you choose, whatever your hours are, we tend to think of this as something that’s just so incredibly simple. But it but it’s not having a job. Takes skill. It takes preparation. It takes professionalism. It takes it just takes a lot of things.

Rachel Star Withers: Mm hmm.

Gabe Howard: We tend to paint them all in the same brush, but not every job is the same. Not every job pays the same and not every job needs the same skill set. So to just throw out the statement, oh, anybody can get a job. Well, a job doing what?

Rachel Star Withers: Now, of course, the opportunities, just like the city versus the country thing, there may be a lot less opportunities, especially if you’re having issues traveling and you live out in the country, you have a lot less jobs that you could even apply for. One of my biggest things is I’ve had some horrible jobs, but I loved the people I worked with. And it was like a joy to go to work because of the people and same things. I’ve had some jobs that some people might consider. Oh, God, you must have loved doing that. I’m like, no, because I hated my boss. I hated who I had to work. Like they made it intolerable. And there’s so many factors that do go into it. I think whenever you have a mental disorder, you’re dealing with that plus medication side effects constantly changing, plus your symptoms constantly changing. And then, of course, your own family life.

Gabe Howard: We’ve discussed on the show before that having a very supportive family is helpful in all areas, is having a supportive family helpful to being employable? To working?

Rachel Star Withers: Yes, especially whenever you’re talking about starting something new or going back to work after, you know, let’s say some sort of breakdown, having to take like a break from it, you might have to lean on your family for a lot of different help. Financial help has been my biggest one, where I became very sick and I had to quit jobs and I had no money coming in for a very long time. And if I hadn’t had the support of my family, I would’ve been homeless. I would have been out of luck.

Gabe Howard: For me, I was very fortunate. I never needed financial help from my family, but what I did need is it. When I went to the psychiatric hospital, when I was off work to seek treatment, I’d be off work for four, six, eight, 12, 16 weeks at a time. And then one day after not having worked for that long, it would be time to go back to work. So here I am, you know, bipolar disorder and an anxiety disorder. And just getting over whatever kept me off work for that long. Now it’s that Monday morning and here I am wide eyed and terrified to go to work. And every single time a family member or a friend drove me to work, they helped me wake up in the morning. They put me in the car. They drove me there. They walked with me into the lobby. Or, you know, depending on the job is as close as they could get. And then they would pick me up from work. They would agree to have lunch with me. And sometimes this would go, you know, multiple friends and multiple families, somebody dropping off, somebody to pick me up. But that was so incredibly helpful because I knew that support was so close and I didn’t need them for anything, but I didn’t care. That made a world of difference in me returning to work. How do you feel about that? Like, how can family members be more supportive in the helping us get over our fear?

Rachel Star Withers: Just talking and I don’t mean, you know, pushing so much to get a job, but just talking to you. My parents are great about asking me, hey, what did you do or you have any stories? What’s been going on? You have any interesting people you’ve met are interesting projects. What are you up to? And just kind of like getting me to talk about work. I’ve noticed just kind of helps me become more confident, even if I’m not so confident while I’m there. My parents like my biggest cheerleaders with that kind of stuff. You know, whenever you have a breakdown, everything kind of is scary afterwords. It can be scary to just like go out to eat. You’re overthinking everything. And if you have anxiety or if you are having hallucinations or delusions worried about other people are looking at you, you’re doing things weird, especially if you’ve been on some certain medications, you might have developed tardive dyskinesia with the shaking minus shaking a lot. And having to start a new job can sometimes be embarrassing because I look like I’m terrified. I’m not I’m just like shaking out of control. I’m dropping things. And I obviously feel like I have to address it right away. And all of that can really just be a lot for anyone. You know, whatever job you’re thinking about doing, you know, just trying to shop and fill out applications can be very intimidating. In the past, you know, my mom has went with me on a couple different ones just to to help me check out the places, say, hey, you know, yeah, I could do this. And she’s like, all right, you know, that new place you could walk to that job like you could. And that’s nice. You know, when you do have kind of that gentle push.

Gabe Howard: But that general pushes is it’s very valuable because on one hand it’s saying, hey, you should do this because it will benefit you. But on the other hand, it’s also saying, I believe that you can do it.

Rachel Star Withers: And now, a word from our sponsor. It can sometimes feel like another schizophrenia episode is just around the corner. In fact, a study found that patients had an average of nine episodes in less than six years. However, there is a treatment option that can help delay another episode, a once monthly injection for adults with schizophrenia. If delaying another episode sounds like it could make a difference for you, or your loved one, learn more about treating schizophrenia with once monthly injections at OnceMonthlyDifference.com. That’s OnceMonthlyDifference.com. And we’re back talking about working with schizophrenia.

Gabe Howard: How do you feel about volunteerism as a path to employment?

Rachel Star Withers: I think that, you know, a lot of people who get nervous when it goes when it comes to going back to work and maybe you flat out can’t or you’re like, rich, I can’t even do a part time job. Volunteer work is great. Anything that gets you out and moving. I pretty much always been involved in some sort of volunteer work. Right now, it’s super fun. I dress up as Spider-Man for the local children’s homes and I love children, so I don’t want them, but I like their happiness. So I love like doing any kind of volunteer work with that. Collecting books if you’re out there and like you love animals. Oh, my goodness. All of the shelters, I know the ones by me. Have these programs where you can volunteer to come and walk the dogs makes you feel so good to actually be helping out.

Gabe Howard: Yeah.

Rachel Star Withers: And then, of course, if you have something you want to work towards, consider internships and apprenticeships. You know, sometimes you can flat out ask people, hey, can I shadow you on the job? And that’s a really great way to kind of put your foot back in the working pool and kind of just. Even though you’re not getting paid for it, kind of get to contribute and do some cool things. So am I like really neat jobs? I’ve done have all been like interning or shadowing different entertainment people where I straight up just e-mailed or called them, got their contact info and was like, Hey, I saw you’re shooting a movie. I was wondering could I come out and shadow you for a few days and you’d be surprised how many people actually respond back like, oh yeah, sure. Come on down.

Gabe Howard: It’s 2019 now and obviously we’ve discussed the benefits of volunteering. But, you know, sometimes it’s just it’s nice to make a buck. And hey, the Internet provides.

Rachel Star Withers: Yes, one of the most amazing things to me is how easy it is to get like your own job where you’re like your own boss through these apps. I have a friend who actually does really well. But pet sitting, that’s all she does.

Gabe Howard: And she uses an app to do it. And of course, we’re all familiar with Ride shares.

Rachel Star Withers: Yep.

Gabe Howard: Probably the most popular hustle side hustle.

Rachel Star Withers: And I love the ones where you’re paid to go pick up someone’s food and take it to them. One of my friends who has severe autism. Well, if you were to meet him, you’d be like, OK. Yes, something’s off. But he can totally drive fine. And he does that for a few hours every day. You know, when he’s feeling good enough to do it and his parents pretty much kind of keep tabs to make sure he’s OK, but that that’s his job. And it’s something he can do completely on his own. And if he has to take a day off because of issues, OK? He just doesn’t do it. He doesn’t log on. And that’s just so cool that we have this ability to kind of pick up all these like little baby jobs.

Gabe Howard: Now, let’s talk about accommodations, because accommodations work in all kinds of ways. There’s reasonable accommodations. There’s unreasonable accommodations. There’s legally required accommodations. And all of this starts with you self advocating because your employer is not going to walk up to you and say, hey, I think you might need X, Y, Z accommodation.

Rachel Star Withers: You don’t sometimes know what you can and can’t ask for. I was in college and there’s like a whole part of the college devoted to that, and I’d never known that until I was in my third year of college and having major issues with brain damage. And I was like, oh, I can come here and you can help me? And that’s when I learned about it. Oh, wait. I can do the same thing on jobs. And from there, I’ve been able to either work with my boss or H.R. on certain things. One of my biggest is that I can’t deal with money. Anything with numbers. I get very confused. Let’s say you give me 20 pennies and tell me to count them. I might come up with a different number each time. I can’t explain why. If I’m just doing even just basic, simple math, I start getting confused. So I’ve had to be very open. Now keep in mind, I’m not applying for jobs at banks.

Gabe Howard: Right. Because you’re aware of this.

Rachel Star Withers: Right. Yes, I’m not being ridiculous when I’m like, you know, oh, I got this job at the bank, by the way. I can’t do anything here. I’m just going to sit here.

Gabe Howard: Because that would be an unreasonable accommodation.

Rachel Star Withers: Oh, right. Yeah. They’d be like, why did you even waste our time? I am very open about it. So that when I do apply for a job, if I find out there’s gonna be a situation like I know right up in the interview, I usually will say something. And then let’s say after I get hired, they change it. Not usually. What happens is as you work for some place for multiple years, they’ll change your position. So suddenly they had me at the cash register and I had to go and be like, I’m really sorry if you remembered when I was hired three years ago and they were like, Oh, wow, Rachel, we totally forgot. And, you know. Yeah. You can’t expect employers to always remember little things about you. So I brought it up and they immediately just kind of adjusted the schedule so that I never worked the cash register alone. I always had someone there.

Gabe Howard: Rachel, it sounds like a lot of your your jobs and a lot of your career have been for smaller businesses, you know, 25 employees or less if you work for a large company. What should you do?

Rachel Star Withers: All large companies should have an H.R. Human Resources go to them and talk. And it’s really good and you’re gonna feel more confident even in just talking if you have like doctor’s note or something like that, kinda to back up what you’re saying. If you don’t want everyone to know, just go to talk to H.R. or a boss or whoever you might have to and just be like, oh, by the way, I have this, this, this and this. You usually don’t have to even disclose your diagnosis, but it’s good if you have some that says, “Hey, this person has trouble with certain things.” One of my doctors actually wrote down options Rachel struggles with at the time. I haven’t really bad memory issues in a he’d written down three different accommodations that maybe they could look into working with me over. So I actually had like these suggestions there and I sat down, I talked with the boss kind of thing. And, OK, here’s what we’ll do. We’re gonna try this for two weeks and they’re like, let’s see how this goes. Especially when you are working for smaller businesses, you know, there’s different things that can happen. I wish I could say all of the jobs I’ve worked. They were incredible and worked with me at all, Rachel. That’s fine. And we’re a very open workplace. But that hasn’t happened. I have definitely had some bad run ins with jobs and whatnot. And sometimes you are all you can do, though, is speak up for yourself. You do have to advocate for yourself. Don’t just keep getting miserable. Speak up, document everything. Emails. If they said, OK, hey, we’ll do this, write it down.

Rachel Star Withers: Even a hey, can I get that in writing and just keep it for your own kind of personal info. I still have the doctor’s recommendations from back when I was in college years and years ago. And while it’s not the best thing that you know, if you’re in a bad situation and it’s hurting, you mentally, quit. It’s going to get harder. That is one thing Michelle talked about. She had to step away from working at those big firms. I’ve had to step away even on small part time jobs, because it was just a really bad atmosphere for me mentally. It’s one reason I like working part time jobs and pushing it to other people with mental disorders, because if you’re working at the snow cone stand for 15 hours a week. Quitting is not going to ruin your career. Like I’ve blown through a lot of part time jobs. It’s not like I have to list them all on a application like, well, I worked three months here at the snow cone. I worked at the baseball stadium on and off for like if you are just trying to get your foot back in the water, and you’re like, hey, this is not a good situation for me. Find another one. You might absolutely love working at the sub shack. Okay? Because you might get to be like, oh, hey, I get free subs and I’m having a good time. I like my employees. And this is an easy job. And you know that not everything has to be prestigious. You can just do things that make you feel good about yourself. And that’s not bad.

Gabe Howard: And that’s also the path to getting to something that is. I’m going to say more prestigious. Nobody starts at the top rate. You start at the level that you can start and you make incremental change and you keep building up when somebody is interviewing for a job. And I don’t care if it’s at a large firm or if it’s at a smaller place. Do you tell them in the interview that you’re a person living with schizophrenia or that you have a mental health condition?

Rachel Star Withers: I personally do not mention anything until after I get the job. Unless during the interview they flat out say something that I know is gonna be an issue. So they flat out say, oh, and you’re gonna have to be counting a lot of money. Can you do that? I’m not gonna flat out lie and be like, yeah. And then the next day after I get the job, “Oh, I was just kidding. I lied yesterday.” So I am. I’ve always been incredibly open about that. If there is any like thing that just flat out I know I’m going to have a problem with.

Gabe Howard: And to be clear, you’re not required to do so, disclosing a health condition is not something, whether it’s mental health, whether it’s mental illness, whether it’s physical disability, whether it’s anything, they’re not allowed to ask you about that and you are not required to tell an employer. So you can choose to. That is absolutely your decision. But I don’t want anybody listening to this to think, oh, well, you’re keeping it from them. That’s not okay. No, it’s absolutely OK. But obviously, you can’t get an accommodation unless you tell your boss or human resources.

Rachel Star Withers: You know, Gabe, if you work at a larger corporation or company, you don’t even have to tell like your boss or supervisor, you go straight to H R and they deal with that. You also like don’t have to tell people exactly what you have. Like, well, I have schizophrenia or I have schizoid personality. Like I many times will just kind of keep it vague as I have a brain disorder and people he’s like, oh, OK. Very few people follow up asking questions about that. My doctor’s notes, they usually don’t say anything specifically like, oh, she has schizophrenia. It’ll say she has usually some sort of mental disorder and it’ll be worded that way, but nothing specific. That’s another thing, too, is you can be vague with people. If your co-worker flat out ask you something, you don’t have to tell them.

Gabe Howard: Especially a co-worker,

Rachel Star Withers: Yeah. Yeah.

Gabe Howard: You don’t have to tell your co-worker anything. I can understand people thinking that they might have to tell a supervisor that that’s your boss. But yeah, you’re not required to disclose anything to a co-worker and you’re not required to disclose health conditions to a supervisor. And the only way that you would need to disclose health conditions to human resources is if you’re asking for that accommodation. Otherwise, it’s your business.

Rachel Star Withers: Yeah, and I will say this. I know that times when I’ve had to take off and then come back. Yeah, sometimes co-workers can just flat out ask you things they shouldn’t. People can be kind of rude and usually I’ll just say, oh, wow, yeah, I’ve been sick and I’m like, OK. Like, I just say sick. I thought, well, I had a mental breakdown and I was wanting to kill myself. And I was so absurdly depressed, like I just said, oh, I was really, really sick. And people like, oh, OK. And they kind of stepped back like, oh, god, how are you? Are you better? I’m like, yeah, I’m good. Like, OK, I do. I’ve gotten to the point sometimes where I’ll, like, practice what I’m going to say if I’m asked if someone brings up, hey, you know, I heard you left work the other day and you were talking to yourself, what went on like, you know, I just had this really bad headache and I was just so hard to think clearly. And people always like, oh, OK. Yeah, no, I’ve had some bad migraines, too. Like, yeah. Yeah.

Gabe Howard: It is amazing how quickly people want to tell their story on top of yours. It’s important for people like us to know that people aren’t actually all that concerned with us for the most part. We think that everybody is like, oh, Rachel left work and they’re all having like meetings about it. In actuality, they just kind of noticed it. And as a point of curiosity, they brought it up to you. Rachel, you had the good fortune to interview Cheryl Wallace. Can you tell us about that?

Rachel Star Withers: A few years back, I got to meet Cheryl Wallace. She reached out to me and she is the V.P. of programs at Rose Hill Center, a mental health facility. They do mental health rehab and also have these work programs pretty much helping you come back from big breakdowns. Got to go there for a few days. I toured the facilities. They’re amazing. And I got to learn all about their programs and different things. So I was so excited that she had time for us for this interview.

Rachel Star Withers: Hello, Cheryl. So tell us a little bit about what Rose Hill is.

Cheryl Wallace: Rose Hill is a residential program for adults who have a mental illness. We are on about 400 acres and we are located in Holly, Michigan. We are a a volunteer program. And we are not a locked unit. So people are living on our campus, but they are able to come and go as they wish.

Rachel Star Withers: And how is Rose Hill different than, let’s say, a standard mental health hospital?

Cheryl Wallace: Rose Hill Center is a residential program and we have folks who come and live here for six to eight months. It’s long term. It’s not a place where you go and take care of an acute illness that’s going on in the moment. But it is basically an opportunity to change your pathway to to manage your symptoms, to be in recovery and learn how to live a fulfilling life. We have individuals from all over the country that come to Rose Hill, so we have a work component on our campus and then we help people move out into the community to volunteer, go to school or work in the community while they’re living here at Rose Hill.

Rachel Star Withers: And can you tell us more about the work programs that you all do?

Cheryl Wallace: We have a structured program so probably five to six hours a day. People can choose to be in one of our work crews. When people first come to Rose Hill, they make a choice on what area they might like to work in. We have a kitchen management crew which basically makes breakfast, lunch and dinner for all of the residents. They work with the chef and they work in a kitchen that is like a restaurant quality kitchen. The second team we have is our horticulture team and we have four big greenhouses on our campus. We have a butterfly house. They also take care of the grounds and to learn about basic taking care of flowers and plants and vegetables and things of that nature. It’s very rewarding to get your hands in the dirt and make something beautiful bloom. So it’s a very popular crew. We also have a farm crew and our we have a fully functioning farm. And then the last area that people can work in is our housekeeping crew, which helps keep all the infections down, cleans the common areas of the different buildings that we have. And we also have about 10 people working on that crew. We have a lot of buildings here.

Rachel Star Withers: When you have clients, do you ever have issues with someone being scared or hesitant about working again?

Cheryl Wallace: All the time. One of the reasons why you get so much benefit from this type of a program when you get to feel comfortable going back into the workforce with a lot of support. A lot of safety nets around. People come to Rose Hill, a lot of times, it’s after an acute episode in their illness. And so they’re very afraid of not being able to do something that they used to do or not feeling confident. There’s a lot of fear that goes on, especially with people who have a diagnosis of schizophrenia. They may have paranoid thoughts or some negative symptoms of not being able to motivate. And so here at Rose Hill, we would take all of that into account. We help people to manage the symptoms and their medications and we slowly work them back into the workforce with lots of handholding and support and then generally increase their responsibility as they feel comfortable to do so. It’s really a challenge sometimes to think, well, I’m just going to get up and go take care of this like nine to five kind of job. And we recognize that people have a lot of symptoms that they need to get under control or at least feel comfortable with before they add on more stressors of a job. We start there, we start on our cruise so that people feel confident they have increased responsibility. I mean, it’s fun. They really enjoy working with the different members of their team and with the animals or work in the kitchen or whatever area they are in. And then as they become more confident and feel like they want to go out in the community, we have different stages. And when they get to Stage 3, we encourage people to work with their vocational coordinator to either volunteer or go back to school. And then once they’re doing that, we try to get them up to about 20 hours a week. And then once they’re confident in that we will also assist them with getting a community job if they feel that that’s what they’d like to do.

Rachel Star Withers: Awesome. Have you found that there’s any general type of work that people respond to with schizophrenia or any other mental disorders? As far as getting back into the workforce?

Cheryl Wallace: I think a lot of times we find with people who have a diagnosis of schizophrenia that starting out with a physical job usually works better for them to get back in the pace. If you are trying to manage maybe some of your delusions or voices or something of that nature, sitting in the sedentary jab kind of allows for a lot more time of concentration. Sometimes people who have a diagnosis of schizophrenia get ill when they’re younger, you know, in their 20s or in college. And so they’ve never really had the opportunity to hold a full time job. So for those folks, it’s also learning what that means. They are perhaps have been stunted at that age or having to really deal with those challenges for a while. And so learning what it means to hold a job. Work with other people. Take direction. All of that, something that we do here at Rose Hill as well.

Rachel Star Withers: And how have you seen people change as they go throughout the program?

Cheryl Wallace: This program is amazing. I mean, simply amazing we have success story after success story when somebody really dedicates themselves to wanting to be able to manage the symptoms with a life worth living. All of those pieces, then we can give them the support and they get the challenge of, OK. These symptoms are happening. And how would I manage that without going back to the hospital or without stopping my medications or whatever? And they learn that they can be really successful in managing that and that gives you confidence and comfort. And I mean, we have people that have been through a program that came here that were really unable to participate or engage socially or we’re very, very frightened. Perhaps some medicines weren’t working very well. And when they leave here, they’re living on their own. They have good relationships. We’ve had people that come through our program who are now E.R. nurses or accountants or I have one guy that’s running a Habitat for Humanity because he wanted to give back to the community. I mean, we have people that just work in the stores and that that’s good for them or just continue to volunteer and help in their community. So it’s amazing. Stable, happy, good relationships, all the things that we all want in life, very, very possible. It takes hard work. It really does. But I think most people that come through our program leave very successfully.

Rachel Star Withers: Thank you so much. Thank you for that information and thank you for all the work that you guys are doing over at Rose Hill.

Cheryl Wallace: And I just want to thank you for letting me have the opportunity to talk with you.

Rachel Star Withers: I love how she brought up the different types of work programs they have. I feel that I would want to be with the animals, and if I wasn’t able to work with the animals, I would do the cleaning crew because I love sometimes just like a good menial task where I can just blast music and just being left in my own world. I feel like those would be the two I gravitated towards.

Gabe Howard: I wish that there were programs like this all over the country, right? I mean, I think that they provide a lot of experience, balance, value. I think that they get people out of their own heads, out of their own homes, out of their own situations and position them to do better. I sincerely hope that if anybody listening to this has one of these in their area, absolutely take full advantage of it. And if you’re ever in a position to advocate for a program like this, please do so, because getting back to work has made all of the difference in my life. And you know, Rachel, you and I talk to hundreds of people in our job and they all describe that working gives them a sense of purpose and value, not because they have mental illness, not because they have schizophrenia, not because they’re living with a disorder, but because every single human on the planet immediately introduces themselves as this is my job.

Rachel Star Withers: Very true. I’m 34 years old and it definitely comes up. You know, I’ll see someone from high school, but I’ll run into someone that, you know, is a family friend. Well, what’s Rachel up to now? What are you doing? And sometimes, you know, I feel bad that I don’t have a better answer. Like. Well, you know, I’m really successful working at such and such or. Oh, well, I’m married with two kids. Like, I don’t have that. Well, I work in entertainment and I live with my parents in the basement below. That’s why I’m here as you guys stopped by. You know, I feel really bad. I hate having to tell you, like, oh, where do you live? And I’m like. Why does it matter? Why you asking? Because I like, oh, well, I put myself down. And I think people in general, we always put ourselves down and we don’t have to. You know, it’s OK to be like, yeah, well, right now I’m just working a part time job doing such and such. I’m focusing on myself. I’m focusing on bettering myself.

Gabe Howard: But it sounds like some of this is the judgment that you put on yourself. Like you said, they’re not actually asking that. That’s just what you heard.

Rachel Star Withers: Correct. Mm hmm. And one thing I liked that Cheryl said was, and I’ve never thought about it until right in that interview was that a lot of us we didn’t go the normal route. You know, we had breakdowns in our late teens, early 20s, which if we had it, you tend to graduate high school, go to college, start working full time. That was kind of what my brother’s route was. Went straight to college, started working and then decide to do military. So working full time the military, whereas me, I had a really rough time after high school for a few years, had some major breakdowns, finally got terrified. I went from being straight A’s on a full scholarship and then being terrified to actually start college thinking I couldn’t handle it even though I was on a full scholarship. I didn’t think I could handle it. Just being terrified to have to sit in a classroom and going back and doing that instead of four years. It took me over five because again, halfway through had another major breakdown and then I barely made it out just because it was so hard and college just finishing it was a weight off my shoulders, but I didn’t have any energy then to enter the workforce and I had another breakdown. And so when she said that, I was thinking, Oh, she’s right. I never learned how to work a 9 to 5 job. Even my college, I would say, was not a normal in any way college experience because it was so scattered and broken up just trying to make it. And that made me feel a little bit better about myself. When she said that because I felt less of a failure, you know, I’m like, yeah, my brother did have it easier.

Gabe Howard: Well, it’s very true. And to be fair, it’s not just high school college, it can be high school, trade school, high school, interning, in high school, getting your first job, high school, military. But the one thing that is certain is that when you’re a worker in your early twenties, your late teens, early 20s. Supervisors are willing to give you more benefits of the doubt. They’re willing to give you more on the job training. They’re willing to give you a little more latitude because they understand that when they were 20, they did boneheaded things and made mistakes. They’re not willing to give that same leeway to a 30 year old because they think you should have learned it by now. But as Cheryl pointed out, and as you just said, when all of our peers were learning how to join the workforce at 20, we were trying to survive. We were trying to get a diagnosis. We were trying to get well. And yeah, that made me feel a lot better, too, because, yeah, we overcame a lot to be here and we deserve credit for that.

Rachel Star Withers: Yes, sometimes, like, we forget how awesome like we are, what it takes to come through things, when I think back, you know, there were days that I lost the ability pretty much. I remember standing there having to get ready for work and I couldn’t remember how a zipper worked. And it was like 30 minutes and it was just like that piece of the puzzle was missing. And I’m just trying to like figure out how a zipper worked. I’d already graduated college. It was summa cum laude. It you know, and then I’m standing there a few weeks later not knowing how to zip up my jacket. And yeah, like when you think like, wow, some of us have really come through a lot where you had to relearned how to socialize with people. You had to re learn how to be able to wake up every day, take a shower and eat breakfast. And if you’re out there listening, you don’t have a mental disorder. You know, maybe you’re a caretaker. Sometimes it can be frustrating like, well, why won’t this person just take care of themselves? Why won’t they just get up and, you know, do this thing? You know, sometimes it’s next to impossible. Like taking a shower, once a weak, sometimes is a major feat because it’s like a giant dark cloud is in your brain and everything’s harder. And to look back at how bad sometimes things were. And somehow I still managed to hold down a job that was even 20 hours a week. I’m like, how did I do that?

Gabe Howard: But you did it. We have to remember to give ourselves credit for that, because we tend to focus on the things that we lost, the times that we lost, the opportunity that we lost. The fact that it’s harder for us to get a job where we’re super ready to focus on that. But the fact that we have survived in an area that other people didn’t even have to compete,

Rachel Star Withers: Yeah.

Gabe Howard: We need to give ourselves credit for that, too.

Rachel Star Withers: I would you know, right now that whatever you’re doing, it’s totally fine. Don’t put yourself down if you can only volunteer one day a week at the church. You know, in your neighborhood, then that’s something that’s you getting out, even if it’s. Well, Rachel. I didn’t get out this week. All I did was I set up an account on an app to maybe start walking dogs. Hey, that’s something. Any little step, you know, we’re not all on the same race. And you can’t look around and compare yourself to other people who they didn’t have a mental breakdown. They didn’t have to repeatedly start over. We like to compare ourselves, like, to someone else who’s also our age that maybe graduated from high school the same time as we did. You know, I’m like, man, they got like a wife and kids and they have like this full time job. And this $300,000 house. And I’m the opposite in every way possible. But you had to start over like five times, you know, and they didn’t. They never had to. So you have to see like where you’re at is sometimes so much more impressive, the more someone else’s because of what you had to do to get there. Thank you so much for listening. We’ll be back next month. But please, like share, subscribe. If you have friends out there who you think would love to hear this podcast, need to hear this podcast, please send it over to them. Thank you so much for listening.

Announcer: Inside Schizophrenia is presented by PsychCentral.com, America’s largest and longest operating independent mental health website. Your host, Rachel Star Withers, can be found online at RachelStarLive.com. Co-host Gabe Howard can be found online at GabeHoward.com. For questions, or to provide feedback, please email talkback@PsychCentral.com. The official web site for Inside Schizophrenia is PsychCentral.com/IS. Thank you for listening and please share widely.

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How Youth Sports Can Help Shield Every Kid—for Life

A National Youth Sports Strategy to increase physical activity among America’s kids is slated to come out of the Department of Health and Human Services (HHS) this month—and it can’t come too soon.

The reasons that our kids should participate in sports are many—from boosting cardiovascular health, to  helping them develop self-control, to the positive impact that exercise has on academic performance

But today, the most pressing reason to encourage sports participation among our youth is their mental health.

Our kids are struggling—and the data isn’t looking good.

Suicide is now the second leading cause of death for America’s youth—spanning the precious ages of 10 to 24. The number of suicides for 10- to 14-year-olds has more than doubled since 2006. And every day, on average, 30,041 high schoolers—grades 9 to 12—try to end their lives. 

Overall, more U.S. adolescents and young adults are experiencing serious psychological distress, major depression, and suicidal thoughts—and more have attempted suicide and taken their own lives, a recent study reveals. Researchers—who compared data from the late 2010s and mid-2000s—believe there’s been a generational shift in mood disorders and suicide-related outcomes. These trends are weak or nonexistent among adults 26 years and older, they say.

The numbers attached to the study are even more unsettling. In the years between 2005 and 2017, there was a 52% increase in 12- to 17-year-olds experiencing symptoms of major depression. Worse yet, between 2008 and 2017, suicides among 18- to 19-year-olds jumped 56%, suicide attempts among 20- and 21-year-olds increased 87%—and there was a 108% surge in 22- and 23-year-olds attempting to take their own lives.

Mental health and what influences it is extremely complicated and multifaceted. And much of what feeds—or strains—the mental and emotional well-being of our youth is deeply entrenched in genetics, culture, environment, experiences and issues of the day.

But exercise is at least one powerful shield—and fortifier—of mental health to which all children, adolescents and young adults should have access. In a world that often feels outside of our control, as a society, we do have the means to provide to our young people the opportunity, resources and support for regular physical activity.

A compelling lineup of research links exercise to resilience, the ability to cope with stress, and emotional health. One meta-analysis of 33 clinical trials found that resistance exercise training—weight lifting—was associated with a significant reduction in depressive symptoms. Another found that physically active adults had fewer days of poor mental health—especially those who participate in team sports. Still more research shows physical inactivity as a risk factor for depression and anxiety.

Researchers from the University of Vermont Medical Center have even gone as far as suggesting that mental health facilities have gyms onsite and that health providers prescribe exercise before psychiatric medications.

Of greatest relevance, perhaps, are the findings released just last month that team sports provide the greatest mental health benefits of any other extracurricular activity, including individual sports. The researchers—who looked at the impact of exercise on kids in the fourth and seventh grades—believe the sense of peer belonging fostered by team sports is what gives it the added edge over other forms of exercise.

What’s more, researchers found that higher levels of sport and physical activity were associated with more positive mental health in undergraduate college students, with Division I athletes experiencing the highest scores. Not surprisingly, as physical activity levels dropped, so did the mental health scores, with the lowest among the physically inactive students. Campuses can raise the overall mental health of students by promoting physical activity, the researchers believe.

Yet, the number of 6- to 12-year-olds regularly playing team sports has fallen to 38%―down from 45% a decade ago.

The science on exercise and the positive impact that team sports can have on youth of all ages is clear. The challenge is accessibility.

All youth of all socioeconomic backgrounds, living in all parts of the country, and of all physical abilities and skill levels need easy opportunity for participating in team sports. That means eliminating barriers like pay-to-play and reining in the hypercompetitiveness that has come to dominate youth sports—stripping them of the inherent fun and eliminating any openings for those who’ll never be on the sports scholarship track.

Almost 3 out of 4 kids (70%) drop out of team sports by the time they’re 13—because it’s no longer fun.

We need to rethink how we can use team sports to bolster the mental health and well-being of our children—because, really, the greatest benefit that team sports offer is their capacity to help prepare our youth for managing all that life will throw their way.

Very soon, HHS will unveil the National Youth Sports Strategy. Chances are, the timing had nothing to do with September being National Suicide Prevention Awareness Month—but it is apt.

I look forward to what HHS has to say. But regardless, each of us needs to come up with solutions—in our own backyards, neighborhoods and communities—for how we can make every kid a welcome, participating and confident part of the team.

We owe them that.

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Do Our Neighbors Matter to Us Anymore?

When I was growing up in my small town of Dunmore, Pennsylvania, neighbors were part of my everyday life. During the summers, the first thing I’d do everyday was head outside to see who was around, then spend the rest of the day playing with the other neighborhood kids. 

That was back in the 1960s and late 50s. It wasn’t just the kids who were friendly with the neighbors back then. The house where I lived had a patio and many evenings, after dinner, grownups from the neighborhood would gather there to chat and relax. 

I could sense that things were different when I was writing my 2015 book, How We Live Now: Redefining Home and Family in the 21st Century. Sure enough, I found this:

“A national survey ongoing since 1974 has shown that Americans have never been less likely to be friends with their neighbors as they are now. The lowest levels of neighborliness were recorded in the suburbs.”

Generations of children grew up hearing Fred Rogers, of Mister Rogers’ Neighborhood, ask, “Won’t you be my neighbor?” This November Tom Hanks will star in the movie A Beautiful Day in the Neighborhood. The documentary Won’t You Be My Neighbor?, released in 2018, was remarkably successful

Is the popularity of Mister Rogers, more than 50 years after the first episode aired, just sentimentality or do neighbors still have a place of significance in the lives of adults in the U.S.? The Pew Research Center conducted a survey in 2018, and just published their results a few weeks ago. One of the most consistent findings was that age mattered. To underscore that, some of the results were reported separately for four age groups: 18-29; 30-49; 50-64; and 65 and older.

1. Most Americans know at least some of their neighbors.

In every age group, more than half (between 54 and 59%) knew at least some of their neighbors. 

2. Older Americans know more of their neighbors than younger ones.

The older people were more likely to know most of their neighbors. Only 20% of the youngest group said they knew most of their neighbors; that number grew to 34% for the oldest group. 

People who were 65 and older almost never said that they knew none of their neighbors. In the youngest group (18-29-year-olds), though nearly 1 in 4 said that — 23%, compared to just 4% for the oldest group. 

3. Among those who know at least some of their neighbors, about two-thirds would trust them with a key to their place.

Averaged across all the people in the survey who said they knew at least some of their neighbors, 66% said they would feel comfortable asking to leave a set of keys with their neighbors for emergencies. That level of trust was identical for the men and the women. 

Again, though, age mattered. Only half of the youngest adults said they would trust neighbors they knew with a key to their place. Many more of the oldest adults — 80% — said that they would. 

Money was also important. Among the wealthiest families (with incomes of more than $75,000), probably living in the wealthiest neighborhoods, about 3 in 4 of them (76%) said they would trust a neighbor they knew with their house key. In the least wealthy neighborhoods (incomes less than $30,000), 58% would be willing to give a key to their place to a neighbor they knew. 

4. People who live in rural areas are more likely to know most of their neighbors. But they are no more likely to have face-to-face conversations with them. 

According to our stereotypes, people who live in cities keep to themselves, while country folk get to know their neighbors. In one way, the Pew results were consistent with those beliefs: only 24% of urban residents said they knew all or most of their neighbors, compared to 40% of rural residents. (Among suburbanites, the figure was 28%.)

But when asked whether they had face-to-face conversations with the neighbors they knew, the people who lived in rural areas were no more likely to say that they did than the people who lived in cities or suburbs. In all three groups, about half said that they had such conversations at least once a week (53% for urban, 49% for suburban, and 47% for rural). 

5. Neighbors communicate in person more than any other way.

Among Americans who know at least some of their neighbors, only 7 percent communicate with them by phone and the same number communicate with them by email or text message. More than twice that many, 20%, say they have face-to-face conversations, several times a week, with the neighbors they know. 

6. Most people never have parties or other get-togethers with their neighbors. 

Asked about attending parties or other get-togethers with their neighbors, nearly 6 in 10 (58%) said that never happened. Still, a non-trivial number, 28%, said they sometimes go to social events with their neighbors, and 1 in 7 do so at least once a month. 

The Pew survey did not ask people whether they were happy with the amount of contact they had with their neighbors. In my research for How We Live Now, I found that people varied a lot in how much they cared about that. People who really wanted their neighbors to be a part of their lives sometimes took pro-active steps to make that happen. They might, for example, initiate events themselves. Sometimes they look for a place to live in which friendly relationships with other community members are known to be valued. Cohousing communities, for example, are built on that principle. In the U.S., there are fewer than 200 cohousing communities, but they are getting more and more attention, so it is possible that their numbers will grow. 

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Lessons on Compassion: Why It’s Good for Us and How We Can Do More of It

A Story of Compassion

Among so much disheartening news these days, once in a while there is a bright spot of news that is truly heart-warming.  Such was the case when I read about, and watched on video 21-year-old Naomi Osaka’s act of kindness and compassion toward 15 year old Coco Gauff at the U.S. Open. After losing in the third round at the U.S. Open, Coco was on the sidelines completely defeated and unsuccessfully trying to fight back tears. Naomi immediately went over to her in this moment of suffering and offered kind words to her, and then invited her to be part of the post-match interview (which is usually only for the victors). During that interview, Naomi became teary as she spoke to Coco’s parents in the audience, recalling being at the same training facility as Coco, and acknowledging Coco’s hard work, and how both they (the parents) and Coco are “amazing.”

Surprising Benefits of Compassion

Interestingly, by expressing compassion, not only does the recipient of the compassion benefit, but so too, does the one giving compassion. Some of these many benefits to the person expressing compassion include reduced levels of cellular inflammation, increased perceptions of happiness and an experience of pleasure, a buffering effect against stress, an increase in longevity, a broadening ability to see a wider perspective outside of oneself, and increasing feelings of social connection (which in and of itself has major implications for health and well-being).

Empathy Versus Compassion

Whereas empathy involves putting yourself in another’s shoes and feeling the suffering of others, compassion goes further and involves a genuine wish or act to alleviate another’s suffering, and to be with another in their suffering.  This was the case with Naomi Osaka. She could have walked off the court and in her own mind recalled what it was like to publicly lose at the U.S. Open (as had happened to her the year prior), and felt in her body what she imagined that Coco Gauff might be feeling, by remembering or imagining the pain of such a moment.  But instead, she went further and reached out in such a genuinely compassionate way, in a moment that Coco will likely never forget, and in a way that likely changed Coco’s experience of her own suffering. Such moments are truly precious and we all have the capacity to offer them. In fact, the impact of doing so may be more far-reaching than you realize.

I still vividly remember such an act of compassion when I was 15. It was at my mother’s funeral, and I recall we were pulling into the driveway of the temple where the funeral service was being held.  My mom had died tragically in a car accident, and it was a time of intense grief and suffering for my family and I. As I looked up through my tears I saw three of my friends from my dance class walking into the sanctuary to be at the funeral.  I had no idea they were coming, and I certainly hadn’t expected them to be there. The fact that they had taken time from their own lives to be with me during this darkest time, to be present with me in my pain, was something I never forgot.

Sometimes, because seeing another person suffering is difficult, we might shy away from opportunities to reach out.  At other times, we might feel helpless because we are not sure how we can make a difference. Other times, people may feel uncertain about how to express compassion.

Where Can We Start?

In these circumstances, where can we start? One place to begin is to look for opportunities for small acts of kindness in ordinary places.  Sometimes something as simple as a smile, a warm gaze, or a small gesture can go a long way. I remember a time when my kids were younger and my son was having a meltdown in the grocery store.  In that moment of frustration and embarrassment for me, someone walking by gave me a friendly smile and an understanding glance as they told me that it wasn’t long ago they too had experienced similar struggles with their child.  That simple gesture went a long way to help relieve my own angst and embarrassment, and to let me know I was not alone. Recently I was in NYC on the subway and a homeless man who had just come on board spoke to everyone in the passenger car, explaining his family’s plight and asking for money.  It was as painful to listen to his story as it was to watch, as every single person in that car looked the other way, as if he wasn’t there. I felt my own inclination to do the same, then fought that urge and turned toward him, looked him in the eyes, and told him that I’m sorry that I had nothing to give him (as I truly didn’t have a single bit of cash on me) but that I wished him and his family well.  I’m not sure that my words made any difference, but I at least wanted to give him an experience of a human connection, as I would have wished for if I were in his shoes.

Another way that we can cultivate compassion is through the meditation practice of loving-kindness.  It turns out that compassion, while innate, is also something that can be taught, learned and practiced. In one study researchers found that two weeks of compassion training (involving listening to a 30 minute guided audio meditation) led to more altruistic behavior and brain changes (greater activation in the parts of the brain involved with empathy, emotional regulation and positive emotions when viewing pictures of human suffering), than for those in the control group. The meditation used in the study involved participants repeating the following phrases: “May you have happiness. May you be free from suffering. May you experience joy and ease.” Participants were first asked to picture someone close to them, wishing them these words in a time they have suffered; then they focused on sending themselves these words as they recalled a time that they have suffered; then they sent such feelings of compassion to a stranger, and finally they imagined sending these words toward someone that they have experienced some difficulty with in their life. 

There are many variations of this meditation practice, but the idea is that phrases of compassion are repeated, sent to oneself and/or others, and become the object of attention throughout the meditation. Try it out and notice the positive feelings that emerge from doing this even if for only a few minutes.

Practicing compassion need not take long or add time to one’s day, but it can have big pay-off, both for the recipient as well as for the one offering compassion. Make it a point to find a small way of engaging in an act of compassion this week, and notice the positivity that is generated by doing so.

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This Is How You Can Truly Help Someone in Crisis

“Let me know how I can help.” Chances are you have offered this incredible kindness to friends and family during difficult times. When my husband was arrested, leaving me and my two sons shocked, hurt, and confused, countless angels in my community suddenly emerged, offering this phrase and a supportive hug. I’ve never felt so incredibly fortunate, even while facing what felt like disaster.

And then I was diagnosed with MS.

The generous offer “Let me know what I can do” turned into a huge question mark: What can anyone do to help? What do we really need?

I was overwhelmed. I couldn’t think clearly and I was struggling to delegate effectively. I knew my boys needed support. We were all desperately trying to keep our heads above water emotionally and still make it to afterschool activities. I knew maintaining a normal and healthy routine would get us through things, but it was hard to see how I could do that while I was heartbroken, worried about my kids, and feeling exhausted from a chronic illness.

This is when I learned:

When people are really struggling, sometimes the biggest help you can give them is a specific offer.

That’s what many members of my circle did when they saw me falter, and my family was rescued as a result. Whether it’s a job loss, a terrible diagnosis, a divorce, or some other awful event, there are so many things that you can just go ahead and do—without asking—when someone you know is in a difficult time, and none of them are wrong.

However, some of them proved more useful than others for us. All help helps. But below are some helping hacks I learned from the incredibly generous members of my community as they lifted me and my sons up:

Grocery Gift Cards Are Sometimes Better Than Casseroles.

Grocery gift cards are a wonderful way to tell someone that you are thinking of them and offer a concrete form of help, especially if someone is struggling with a job loss.

As a rule of thumb: Gift cards are better than making a meal unless you are certain that the fridge is empty.

We had so many casserole dishes at one point mid-crisis that we ran out of room in the freezer and I was giving away food to neighbors. It was a great problem to have but I think gift cards are a bit easier for the user. You can always check before you cook. A simple phone call: “Hi! Do you have freezer space, or would a grocery card be easier?” would clear things up in five minutes.

Offer a Specific Outing.

Another great way to help is to offer a friend or a family in crisis an outing. When people are going through a crisis, sometimes it is helpful to pull them out of it and into something distracting and fun. A dear friend took me and my kids to feed the ducks one afternoon amid the chaos. She had it all planned out, with duck food and kid snacks. It was an easy, quick outing that brought us a much-needed change of scenery.

Try a Fun (and Planned) Drop-In.

Just dropping in on someone in crisis isn’t always a great idea unless you are incredibly close, but outings can also be too big to plan and execute. So strike a middle ground: Opt for the planned drop-in. Planning a fun drop-in can be equally distracting and even more relaxing for those who are struggling. A teenaged friend of ours brought water balloons over one hot day and he played in our yard with my kids. Everyone was soaked and cooled off, and watching my boys have a blast running around and playing in our backyard gave me a feeling of warmth and normalcy for a moment.

Send an Old-Fashioned Greeting Card.

These days most of our messages are electronic, but I still think that an old-fashioned greeting card, the paper-and-envelope kind, can brighten someone’s day. Mail a card with a quick note to someone, or leave it on a co-worker’s desk, and I guarantee that the recipient will be pleased with the thought. In the card, you can offer to babysit or do yard work or if you’re not close yet, give your cell number and offer to listen anytime your acquaintance needs to vent.

Whatever You Do, Don’t Do Nothing!

My dad died when I was 21 years old. I recall so clearly being frustrated when well-meaning adults said things like, “I wanted to ask how you were but I didn’t want to bring it up and make you cry.” I had just lost my dad. Of course I was sad and of course I was crying a lot.

It takes courage to ask someone how they are when they are mourning, but please be brave and ask!

Bring up their loved one or their troubles and ask them to tell you about them. When my family went through crisis, our friends checked their shyness at the door. It helped immensely on our healing journey.

There’s no wrong way to help people in crisis, and the bottom line is:

Stay close. Stay in touch. Even if you feel like your connection is distant, it’s possible that that person is struggling alone today.

Reach out. Offer support in a way that feels authentic to you. We each have gifts that we can share with one another. Sharing them with someone at their rock bottom might be just what they need to stay afloat.

This post courtesy of Spirituality & Health.

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How to Build Confidence & Self-Esteem After a Job Loss

Deal with your job loss and bounce back better than ever.

In the midst of unemployment, it’s easy to lose hope and wallow in your low self-esteem, but you can learn how to build confidence again and take back your life.

Losing or getting fired from your job can seem like the end of the world. You might feel disbelief, anger, sadness, uncertainty, fear, and even panic — and these are all normal emotions given the circumstances.

Being unemployed can feel very personal in the beginning.

“Why me? Why now?” you ask.

Companies decide to make structural or personnel changes for many reasons. And while it doesn’t make it right or pleasant, the truth is the reason for your termination doesn’t ultimately matter.

What counts is learning how to deal with this unexpected life change, so you can mentally prepare for re-entering the job market. And there’s no harm in hoping for the best, either.

It’s easy to get stuck in pity and feel discouraged when your self-esteem has taken a hit and your wallet is empty, but there is a reason for optimism.

There are lessons to be learned from this job loss experience and by slowly building confidence, you will have better success moving on when you adopt a positive mindset.

Here are 10 ways to build your confidence and self-esteem so you can have hope again in the face of unemployment.

1. Give Yourself Time to Mourn.

A loss is a loss. Losing your job can cause you to doubt your abilities and put you on shaky ground for the next opportunity. You might even feel paralyzed.

On the other end of the spectrum, I sometimes see clients jump into job search mode right when they’re not ready — they haven’t dealt with their loss. I don’t suggest taking off too much time, but a few days or weeks to decompress is healthy and wise.

Allow yourself to feel whatever emotions come up for you. Recognize that you won’t feel these things forever and you are not alone. If you take some time to grieve the loss of your job, your future in that organization, and your colleagues, you’ll be on the path to healing.

Skip this step and you’ll risk holding onto resentment.

Hold onto the positive experiences you had. In time, the negative ones become a distant memory. Most of all, give yourself some compassion.

How to Help Your Spouse When They Lose Their Job

2. Communicate With Your Loved Ones.

Share your job loss news with those closest to you. I’ve heard stories of newly terminated employees dressing up, leaving the house every day and pretending they are going to work because they can’t face telling their family.

There is no shame in job loss.

Your loved ones might have their reaction to your job loss and it’s normal for them to have insecurities around it. In a time of feeling loss of control, what you can control is what and how you tell your family.

Let them know that you’re getting support — perhaps in the form of severance, benefits continuance, and outplacement services — and that you can work through this challenging time together. Your job loss may end up being a bonding opportunity for your relationship.

Resist the urge to shelter your kids, also. Teach them about bouncing back and solving problems.

Gradually widen your circle over the coming weeks. You’ll be bound to find others who have experienced similar circumstances, and you’ll realize you’re not alone.

People have a natural inclination to help, too, so when you’re ready, take them up on their offers.

3. Ask for Help.

Consult a lawyer to ensure your severance terms are fair and reasonable, given all the circumstances. Make sure you investigate your health and benefits coverage, also, and make a note of important dates to get in your claims or convert to a private plan.

If your severance package didn’t include outplacement services, consider hiring a career coach to jump start your job search process or asking a mentor for assistance.

An accountability partner can work with you to uncover your strengths, open up new possibilities for your career, keep you on track with your goals, and help you to shift your mindset.

4. Create a Budget.

Concerning your financials, it’s best to take a balanced approach. Don’t go overboard with spending, trying to prove that you’re going to be all right and don’t catastrophize about your financial situation.

Give yourself a spending budget and get creative to make your dollars go farther.

5. Make Time for Self-Care.

Take this time to do things for yourself that you might not normally do. Read a book, indulge in a nap, get a massage or acupuncture treatment. It’s also essential to eat well and take some extra supplements to boost your ability to manage your stress.

Go to the doctor for your overdue physical and attend to your mental health, too. Let your doctor know if you’re having trouble adjusting and it’s interfering with your ability to function.

6. Put a Daily Routine in Place.

Resist any urge to stay in bed all day. Get up at your regular time and create a routine for yourself. Block off time to relax, eat and sleep on a consistent schedule, and go to the gym as usual.

Make sure that you also dedicate time each day for your career transition efforts, which might include reflecting on your strengths and ideal job, and marketing yourself. Consistency is key.

7. Reflect and Focus.

Take the next few weeks to come up with a game plan instead of sending out 100 resumes. Putting in a quality application takes a lot of time and effort. Make sure you’re applying to the right roles in the right organizations, or you’ll get disappointing results.

Success often means digging deep, connecting to your inner wisdom, looking back at your life’s lessons, and projecting forward. Focus on what you love, what’s important to you, and what you can contribute and then create a crystal-clear vision of your future work.

When you do this, you will be in an excellent position to market yourself and your resume.

8. Get Some Perspective.

It may seem like forced time off to lose your job, but you can use this time to take a step back and look at your circumstances with fresh eyes. Get into nature, go near a body of water, or climb up a hill or mountain – a little height can give you a view from a new angle.

Often it helps to speak with someone objective about your situation and realize that your situation is not as bad as you think. You have something unique to offer an employer and the world.

9. Find Joy.

Use this time off to consciously look for happiness in simple pleasures. Reconnect with hobbies like gardening or sports, or reinvigorate your life with music — in fact, singing is scientifically proven to lift your spirits.

Most of all, be mindful of all the beauty that is around you. Inject joy into every day.

How to Cope If You’re Constantly Worried You Might Lose Your Job

10. Be Positive.

You have a lot to bring to a new job, and you’ll find that this period is just a blip in your overall career.

If you’re having trouble believing this just now, write out some affirmations and keep saying them until you are confident they are true:

  • I have amazing talents to offer an organization.
  • I trust myself, and I trust in the universe.
  • I am energized to find my next job.
  • I believe in myself and my ability to do my ideal work.

Here’s the glimmer of hope in your job loss: you’re free!

You’re available to reflect on what you want and take your career to new heights.

If you do these 10 things, you’ll be in a healthier state of mind and ready to land a better-suited job.

So, don’t look back. A bright future is on the horizon.

This guest article was originally published on YourTango.com: 10 Ways To Find Hope And Confidence When You’ve Just Lost Your Job.

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via theshiningmind.com
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